Canonical Allele Identifier: PA2826614511
Gene: HARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 39620
ClinVar RCV Id: RCV000032820 RCV002468984 RCV002513308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265660.1:p.Leu175Val
CA343806
NM_001278731.2:c.523C>G