Allele Registry

Canonical Allele Identifier: PA2826006695

Gene: HNF1B HGNC NCBI

ClinVar RCV:

RCV000030531

ClinVar Variation:

36850

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159395.1:p.Trp171Arg	CA214361 NM_001165923.4:c.511T>C CA398751173 NM_001165923.4:c.511T>A