Canonical Allele Identifier: PA102460
Gene: XPA HGNC NCBI

Linked Data

ClinVar Variation Id: 364088
ClinVar RCV Id: RCV000668335 RCV003237833 RCV003114519
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000371.1:p.His244Arg
CA5148691
NM_000380.4:c.731A>G