Canonical Allele Identifier: PA2828095781
Gene: HARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1438891
ClinVar RCV Id: RCV001949096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350464.1:p.Gln172Arg
CA361197645
NM_001363535.2:c.515A>G