Allele Registry

Canonical Allele Identifier: PA916043776

Gene: HARS2 HGNC NCBI

ClinVar RCV:

RCV000197397

RCV000782168

ClinVar Variation:

214542

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350464.1:p.Lys64Glu	CA321856 NM_001363535.2:c.190A>G