Canonical Allele Identifier: PA2828564920
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1517423
ClinVar RCV Id: RCV002027348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361806.1:p.Val197Met
CA3623681
NM_001374877.1:c.589G>A