Canonical Allele Identifier: PA2826734799
Gene: HNF4A HGNC NCBI

Linked Data

ClinVar Variation Id: 36349

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274113.1:p.Ser118Gly
CA213929
NM_001287184.2:c.352A>G