Canonical Allele Identifier: PA2827547244
Gene: RARS2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337434.1:p.Ile541Val
CA3916190
NM_001350505.2:c.1621A>G