Canonical Allele Identifier: PA2826453940
Gene: HARS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 29756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244971.1:p.Tyr394Ser
CA277969
NM_001258042.3:c.1181A>C