Canonical Allele Identifier: PA2826758316
Gene: HARS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 29756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276021.1:p.Tyr380Ser
CA277969
NM_001289092.1:c.1139A>C