Canonical Allele Identifier: PA2828508874
Gene: FAH HGNC NCBI

Linked Data

ClinVar Variation Id: 887284
ClinVar RCV Id: RCV001119931 RCV002261282
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361306.1:p.His154Gln
CA7691193
NM_001374377.1:c.462C>A
CA393619773
NM_001374377.1:c.462C>G