Canonical Allele Identifier: PA2828041008
Gene: XPA HGNC NCBI

Linked Data

ClinVar Variation Id: 810395
ClinVar RCV Id: RCV000999185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341904.1:p.Glu211Gln
CA374185387
NM_001354975.2:c.631G>C