Canonical Allele Identifier: PA2827022852
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1052874
ClinVar RCV Id: RCV001361138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305801.1:p.Thr121Met
CA3623632
NM_001318872.2:c.362C>T