Canonical Allele Identifier: PA645509779
Gene: HNF4A HGNC NCBI
ClinVar RCV:
RCV000504596
ClinVar Variation:
437910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000448.3:p.Gln277Glu
CA409107507
NM_000457.6:c.829C>G