Canonical Allele Identifier: PA2828041014
Gene: XPA HGNC NCBI

Linked Data

ClinVar Variation Id: 135462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341904.1:p.Arg216Cys
CA162844
NM_001354975.2:c.646C>T