Canonical Allele Identifier: PA645376315
Gene: XPA HGNC NCBI

Linked Data

ClinVar Variation Id: 430367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000371.1:p.Cys108Tyr
CA374187825
NM_000380.4:c.323G>A