Canonical Allele Identifier: PA2826468861
Gene: HNF4A HGNC NCBI

Linked Data

ClinVar Variation Id: 156152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245284.1:p.Arg78Trp
CA170773
NM_001258355.2:c.232C>T