Allele Registry

Canonical Allele Identifier: PA214362

Gene: HNF1B HGNC NCBI

ClinVar RCV:

RCV000030531

ClinVar Variation:

36850

HGVS (amino-acid)	Matching Registered Transcripts
NP_000449.1:p.Trp171Arg	CA214361 NM_000458.4:c.511T>C CA398751173 NM_000458.4:c.511T>A