Canonical Allele Identifier: PA2741919385
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2625111
ClinVar RCV Id: RCV003377790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005422.1:p.Ser22Arg
CA370199511
NM_005431.2:c.66T>G
CA370199512
NM_005431.2:c.66T>A
CA370199516
NM_005431.2:c.64A>C