Canonical Allele Identifier: PA891847371
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 587653
ClinVar RCV Id: RCV000714941 RCV000714919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006558.1:p.His159Pro
CA362735365
NM_006567.5:c.476A>C