Allele Registry

Canonical Allele Identifier: PA2826006897

Gene: HNF1B HGNC NCBI

ClinVar RCV:

RCV000013476

RCV001124747

RCV003153303

ClinVar Variation:

12641

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159395.1:p.Ser439Arg	CA122603 NM_001165923.4:c.1317C>G CA398755783 NM_001165923.4:c.1317C>A CA398755800 NM_001165923.4:c.1315A>C