Canonical Allele Identifier: PA162846
Gene: XPA HGNC NCBI

Linked Data

ClinVar Variation Id: 135462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000371.1:p.Arg258Cys
CA162844
NM_000380.4:c.772C>T