Canonical Allele Identifier: PA2826889012
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 290901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291215.1:p.Ile377Phe
CA8518862
NM_001304286.2:c.1129A>T