Canonical Allele Identifier: PA2827547753
Gene: RARS2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337436.1:p.Ile366Val
CA3916190
NM_001350507.1:c.1096A>G