Allele Registry

Canonical Allele Identifier: PA091994

Gene: HARS2 HGNC NCBI

ClinVar RCV:

RCV000206915

RCV002517027

ClinVar Variation:

208286

HGVS (amino-acid)	Matching Registered Transcripts
NP_036340.1:p.Val368Leu	CA350908 NM_012208.4:c.1102G>T CA361201792 NM_012208.4:c.1102G>C