Canonical Allele Identifier: PA2829584196
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3224695
ClinVar RCV Id: RCV004521385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005422.1:p.Phe241Val
CA370198087
NM_005431.2:c.721T>G