Canonical Allele Identifier: PA2827547838
Gene: RARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 215080

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337437.1:p.Arg83His
CA323244
NM_001350508.1:c.248G>A