Canonical Allele Identifier: PA916076528
Gene: HNF4A HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849181.1:p.Gln277Glu
CA409107507
NM_178850.3:c.829C>G