NM_000190.4(HMBS):c.961C>T (p.Arg321Cys) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 8, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002775901.3
Allele description [Variation Report for NM_000190.4(HMBS):c.961C>T (p.Arg321Cys)]
NM_000190.4(HMBS):c.961C>T (p.Arg321Cys)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
ABC-type oligopeptide transporter ABCB9 isoform 5 [Homo sapiens]
ABC-type oligopeptide transporter ABCB9 isoform 5 [Homo sapiens]gi|339895787|ref|NP_001229943.1|Protein
-
BEN domain-containing protein 2 isoform 1 [Homo sapiens]
BEN domain-containing protein 2 isoform 1 [Homo sapiens]gi|193794843|ref|NP_699177.2|Protein
-
Homo sapiens cDNA clone IMAGE:6501134, partial cds
Homo sapiens cDNA clone IMAGE:6501134, partial cdsgi|49117509|gb|BC073144.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 1, 2024