Canonical Allele Identifier: PA2828564359
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 959450
ClinVar RCV Id: RCV001232805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361804.1:p.Lys406Arg
CA362737082
NM_001374875.1:c.1217A>G