Allele Registry

Canonical Allele Identifier: PA2826614497

Gene: HARS2 HGNC NCBI

ClinVar Allele:

211116

ClinVar RCV:

RCV000199285

RCV000223531

RCV000782169

ClinVar Variation:

214543

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265660.1:p.Arg125Cys	CA323817 NM_001278731.2:c.373C>T