Canonical Allele Identifier: PA2828565256
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2870316
ClinVar RCV Id: RCV003654007

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361807.1:p.His159Tyr
CA362735362
NM_001374878.1:c.475C>T