Canonical Allele Identifier: PA645387562
Gene: XPNPEP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 341668
ClinVar RCV Id: RCV000279640 RCV000863147
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071381.1:p.Ile240Leu
CA10251702
NM_022098.4:c.718A>T
CA411678212
NM_022098.4:c.718A>C