Canonical Allele Identifier: PA2828509035
Gene: FAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2183248
ClinVar RCV Id: RCV002615417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361306.1:p.Cys338Tyr
CA393621758
NM_001374377.1:c.1013G>A