Allele Registry

Canonical Allele Identifier: PA916017165

Gene: HARS1 HGNC NCBI

ClinVar RCV:

RCV000201520

ClinVar Variation:

217508

HGVS (amino-acid)	Matching Registered Transcripts
NP_001276022.1:p.Asp61Glu	CA279336 NM_001289093.1:c.183T>G CA361256011 NM_001289093.1:c.183T>A