Canonical Allele Identifier: PA658807896
Gene: XPNPEP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 538749
ClinVar RCV Id: RCV000677015 RCV001082671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071381.1:p.Pro493Ala
CA10251957
NM_022098.4:c.1477C>G