Canonical Allele Identifier: PA2828565283
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 576093
ClinVar RCV Id: RCV000698505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361807.1:p.Gln193Arg
CA362735586
NM_001374878.1:c.578A>G