Canonical Allele Identifier: PA2826453601
Gene: HARS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 29756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244970.1:p.Tyr434Ser
CA277969
NM_001258041.3:c.1301A>C