Allele Registry

Canonical Allele Identifier: PA2826453382

Gene: HARS1 HGNC NCBI

ClinVar RCV:

RCV000201520

ClinVar Variation:

217508

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244970.1:p.Asp155Glu	CA279336 NM_001258041.3:c.465T>G CA361256011 NM_001258041.3:c.465T>A