Allele Registry

Canonical Allele Identifier: PA321857

Gene: HARS2 HGNC NCBI

ClinVar RCV:

RCV000197397

RCV000782168

ClinVar Variation:

214542

HGVS (amino-acid)	Matching Registered Transcripts
NP_036340.1:p.Lys58Glu	CA321856 NM_012208.4:c.172A>G