Canonical Allele Identifier: PA162843
Gene: XPA HGNC NCBI

Linked Data

ClinVar Variation Id: 135461
ClinVar RCV Id: RCV000122319 RCV000319809 RCV000860760
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000371.1:p.Leu252Val
CA162841
NM_000380.4:c.754C>G