NM_000458.4(HNF1B):c.364G>A (p.Ala122Thr) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 1, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000731660.4
Allele description [Variation Report for NM_000458.4(HNF1B):c.364G>A (p.Ala122Thr)]
NM_000458.4(HNF1B):c.364G>A (p.Ala122Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
RPN2 [Neogale vison]
RPN2 [Neogale vison]Gene ID:122916093Gene
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See more...Assertion and evidence details
Last Updated: Apr 1, 2023