Canonical Allele Identifier: PA110427
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 39824
ClinVar RCV Id: RCV000033044 RCV000162158 RCV000497519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006558.1:p.Tyr144Cys
CA130596
NM_006567.5:c.431A>G