Canonical Allele Identifier: PA170777
Gene: HNF4A HGNC NCBI

Linked Data

ClinVar Variation Id: 156152
ClinVar RCV Id: RCV000144170 RCV000193614 RCV000255966 RCV000763446 RCV000850560 RCV002408643 RCV003993659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274112.1:p.Arg60Trp
CA170773
NM_001287183.2:c.178C>T