Canonical Allele Identifier: PA213918
Gene: HNF4A HGNC NCBI

Linked Data

ClinVar Variation Id: 36345

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_787110.2:p.Ile441Val
CA213913
NM_175914.5:c.1321A>G