Allele Registry

Canonical Allele Identifier: PA2826614515

Gene: HARS2 HGNC NCBI

ClinVar RCV:

RCV000493401

ClinVar Variation:

429211

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265660.1:p.Asp189Gly	CA128342035 NM_001278731.2:c.566A>G