Canonical Allele Identifier: PA915963149
Gene: XPA HGNC NCBI

Linked Data

ClinVar Variation Id: 552532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000371.1:p.Glu245Ter
CA658821481
NM_000380.4:c.732dup