Canonical Allele Identifier: PA916019687
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 635672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291215.1:p.Arg181Gln
CA8519066
NM_001304286.2:c.542G>A