Canonical Allele Identifier: PA2826758613
Gene: HARS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 29756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276022.1:p.Tyr340Ser
CA277969
NM_001289093.1:c.1019A>C