Allele Registry

Canonical Allele Identifier: PA2828095891

Gene: HARS2 HGNC NCBI

ClinVar RCV:

RCV000206915

RCV002517027

ClinVar Variation:

208286

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350465.1:p.Val298Leu	CA350908 NM_001363536.2:c.892G>T CA361201792 NM_001363536.2:c.892G>C