Canonical Allele Identifier: PA2828040997
Gene: XPA HGNC NCBI

Linked Data

ClinVar Variation Id: 552532
ClinVar RCV Id: RCV000667814 RCV001388621
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341904.1:p.Glu203Ter
CA658821481
NM_001354975.2:c.606dup