Canonical Allele Identifier: PA645444107
Gene: PARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 432121
ClinVar RCV Id: RCV000497433 RCV000779609 RCV000723278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689481.2:p.Val95Ile
CA869514
NM_152268.4:c.283G>A