Canonical Allele Identifier: PA913193073
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 595969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000449.1:p.Ala122Thr
CA398751718
NM_000458.4:c.364G>A