Allele Registry

Canonical Allele Identifier: PA2828095793

Gene: HARS2 HGNC NCBI

ClinVar RCV:

RCV000493401

ClinVar Variation:

429211

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350464.1:p.Asp220Gly	CA128342035 NM_001363535.2:c.659A>G