Allele Registry

Canonical Allele Identifier: PA2826888952

Gene: HNF1B HGNC NCBI

ClinVar RCV:

RCV000030537

RCV001844804

ClinVar Variation:

36856

HGVS (amino-acid)	Matching Registered Transcripts
NP_001291215.1:p.Asn295Ser	CA214373 NM_001304286.2:c.884A>G