Canonical Allele Identifier: PA213919
Gene: HNF4A HGNC NCBI

Linked Data

ClinVar Variation Id: 36345
ClinVar RCV Id: RCV000030015 RCV000725499 RCV000764241 RCV001142000 RCV001358754 RCV001844803 RCV003234540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000448.3:p.Ile463Val
CA213913
NM_000457.6:c.1387A>G