Allele Registry

Canonical Allele Identifier: PA111348

Gene: HNF1B HGNC NCBI

ClinVar RCV:

RCV000429473

RCV000787092

RCV002282139

RCV002450971

RCV002467781

RCV003922733

ClinVar Variation:

379811

HGVS (amino-acid)	Matching Registered Transcripts
NP_000449.1:p.Gly370Ser	CA8518897 NM_000458.4:c.1108G>A