Canonical Allele Identifier: PA109950
Gene: XPNPEP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 51
ClinVar RCV Id: RCV000000068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071381.1:p.Gly453Cys
CA113823
NM_022098.4:c.1357G>T