Canonical Allele Identifier: PA1139716256
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 959450
ClinVar RCV Id: RCV001232805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006558.1:p.Lys406Arg
CA362737082
NM_006567.5:c.1217A>G