Canonical Allele Identifier: PA213935
Gene: HNF4A HGNC NCBI

Linked Data

ClinVar Variation Id: 36349

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000448.3:p.Ser143Gly
CA213929
NM_000457.6:c.427A>G