Allele Registry

Canonical Allele Identifier: PA2826614633

Gene: HARS2 HGNC NCBI

ClinVar RCV:

RCV000206915

RCV002517027

ClinVar Variation:

208286

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265661.1:p.Val224Leu	CA350908 NM_001278732.2:c.670G>T CA361201792 NM_001278732.2:c.670G>C