Allele Registry

Canonical Allele Identifier: PA2826006884

Gene: HNF1B HGNC NCBI

ClinVar RCV:

RCV000030520

RCV002464083

ClinVar Variation:

36839

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159395.1:p.Met416Thr	CA214346 NM_001165923.4:c.1247T>C