Canonical Allele Identifier: PA321329
Gene: HARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214545
ClinVar RCV Id: RCV000725134 RCV002517224
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036340.1:p.Ile319Thr
CA321328
NM_012208.4:c.956T>C