Canonical Allele Identifier: PA2828508771
Gene: FAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1685807
ClinVar RCV Id: RCV002249974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361306.1:p.Val21Phe
CA393615587
NM_001374377.1:c.61G>T