Canonical Allele Identifier: PA2827548677
Gene: RARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 402195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337440.1:p.Ser268Pro
CA3916314
NM_001350511.2:c.802T>C