Canonical Allele Identifier: PA320066
Gene: RARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 215067
ClinVar RCV Id: RCV000195702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064716.2:p.Tyr445Cys
CA320065
NM_020320.5:c.1334A>G