Canonical Allele Identifier: PA2827022960
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1427586
ClinVar RCV Id: RCV001945956

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305801.1:p.Ala235Val
CA3623715
NM_001318872.2:c.704C>T