Allele Registry

Canonical Allele Identifier: PA916010575

Gene: HARS2 HGNC NCBI

ClinVar RCV:

RCV000493401

ClinVar Variation:

429211

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265661.1:p.Asp70Gly	CA128342035 NM_001278732.2:c.209A>G