Canonical Allele Identifier: PA2828041011
Gene: XPA HGNC NCBI

Linked Data

ClinVar Variation Id: 1705178
ClinVar RCV Id: RCV002281808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341904.1:p.Tyr215Ter
CA2580080765
NM_001354975.2:c.645_649del