Canonical Allele Identifier: PA111191
Gene: HNF4A HGNC NCBI

Linked Data

ClinVar Variation Id: 156152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000448.3:p.Arg85Trp
CA170773
NM_000457.6:c.253C>T