Canonical Allele Identifier: PA915963151
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_000371.1:p.Glu253Gln
CA374185387
NM_000380.4:c.757G>C