Canonical Allele Identifier: PA103076
Gene: HARS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 29756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002100.2:p.Tyr454Ser
CA277969
NM_002109.6:c.1361A>C