Canonical Allele Identifier: PA2828566530
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 959450
ClinVar RCV Id: RCV001232805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362187.1:p.Lys362Arg
CA362737082
NM_001375258.1:c.1085A>G