Canonical Allele Identifier: PA916043015
Gene: XPA HGNC NCBI

Linked Data

ClinVar Variation Id: 430367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341904.1:p.Cys66Tyr
CA374187825
NM_001354975.2:c.197G>A