Canonical Allele Identifier: PA2573253002
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1517423
ClinVar RCV Id: RCV002027348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006558.1:p.Val197Met
CA3623681
NM_006567.5:c.589G>A