NM_178857.6(RP1L1):c.398A>G (p.Glu133Gly) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 24, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002027723.5
Allele description
NM_178857.6(RP1L1):c.398A>G (p.Glu133Gly)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens cathepsin V (CTSV), transcript variant 1, mRNA
Homo sapiens cathepsin V (CTSV), transcript variant 1, mRNAgi|1519246270|ref|NM_001333.4|Nucleotide
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See more...Assertion and evidence details
Last Updated: Feb 28, 2024