Canonical Allele Identifier: PA2573072877
Gene: FAH HGNC NCBI

Linked Data

ClinVar Variation Id: 596939
ClinVar RCV Id: RCV000732920 RCV002535301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361309.1:p.Val91Met
CA7691069
NM_001374380.1:c.271G>A