Canonical Allele Identifier: PA2828040993
Gene: XPA HGNC NCBI

Linked Data

ClinVar Variation Id: 364088
ClinVar RCV Id: RCV000668335 RCV003237833 RCV003114519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341904.1:p.His202Arg
CA5148691
NM_001354975.2:c.605A>G