Canonical Allele Identifier: PA2830382539
Gene: HNF4A HGNC NCBI

Linked Data

ClinVar Variation Id: 36349

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849180.1:p.Ser143Gly
CA213929
NM_178849.3:c.427A>G