Canonical Allele Identifier: PA162849
Gene: XPA HGNC NCBI

Linked Data

ClinVar Variation Id: 135463
ClinVar RCV Id: RCV000122321 RCV000665473 RCV002260991 RCV002257444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000371.1:p.Arg228Gln
CA162847
NM_000380.4:c.683G>A