Canonical Allele Identifier: PA916019630
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 635723
ClinVar RCV Id: RCV000787242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291215.1:p.Glu78Asp
CA398753631
NM_001304286.2:c.234G>T
CA398753634
NM_001304286.2:c.234G>C