Canonical Allele Identifier: PA2828564182
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 576093
ClinVar RCV Id: RCV000698505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361804.1:p.Gln193Arg
CA362735586
NM_001374875.1:c.578A>G