Canonical Allele Identifier: PA213917
Gene: HNF4A HGNC NCBI

Linked Data

ClinVar Variation Id: 36345

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274112.1:p.Ile438Val
CA213913
NM_001287183.2:c.1312A>G