Canonical Allele Identifier: PA321857
Gene: HARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214542
ClinVar RCV Id: RCV000197397 RCV000782168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036340.1:p.Lys58Glu
CA321856
NM_012208.4:c.172A>G