Allele Registry

Canonical Allele Identifier: PA111432

Gene: HNF1B HGNC NCBI

ClinVar RCV:

RCV000013476

RCV001124747

RCV003153303

ClinVar Variation:

12641

HGVS (amino-acid)	Matching Registered Transcripts
NP_000449.1:p.Ser465Arg	CA122603 NM_000458.4:c.1395C>G CA398755783 NM_000458.4:c.1395C>A CA398755800 NM_000458.4:c.1393A>C