Canonical Allele Identifier: PA916043783
Gene: HARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214547
ClinVar RCV Id: RCV000195916 RCV000767025 RCV002500613 RCV003955189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350464.1:p.Gly375Arg
CA320300
NM_001363535.2:c.1123G>C