Canonical Allele Identifier: PA2828566338
Gene: FARS2 HGNC NCBI
ClinVar RCV:
RCV000239526
ClinVar Variation:
253159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362187.1:p.Asp142Tyr
CA10586223
NM_001375258.1:c.424G>T