Allele Registry

Canonical Allele Identifier: PA916019657

Gene: HNF1B HGNC NCBI

ClinVar RCV:

RCV000787212

ClinVar Variation:

635699

HGVS (amino-acid)	Matching Registered Transcripts
NP_001291215.1:p.Asn146Asp	CA398751462 NM_001304286.2:c.436A>G