Canonical Allele Identifier: PA658749889
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 488360
ClinVar RCV Id: RCV000578201 RCV001246829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006558.1:p.Ala154Val
CA3623648
NM_006567.5:c.461C>T