Canonical Allele Identifier: PA1139743373
Gene: FAH HGNC NCBI

Linked Data

ClinVar Variation Id: 887284
ClinVar RCV Id: RCV001119931 RCV002261282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361309.1:p.His154Gln
CA7691193
NM_001374380.1:c.462C>A
CA393619773
NM_001374380.1:c.462C>G