Canonical Allele Identifier: PA2826453212
Gene: HARS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 29756
ClinVar RCV Id: RCV000022619 RCV000608744 RCV000623702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244969.1:p.Tyr414Ser
CA277969
NM_001258040.3:c.1241A>C