Canonical Allele Identifier: PA2828566389
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1433148
ClinVar RCV Id: RCV001982182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362187.1:p.Arg198Trp
CA362735613
NM_001375258.1:c.592C>T