Canonical Allele Identifier: PA2828564549
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 576093
ClinVar RCV Id: RCV000698505
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361805.1:p.Gln193Arg
CA362735586
NM_001374876.1:c.578A>G