Canonical Allele Identifier: PA1139710198
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 963805
ClinVar RCV Id: RCV001237886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005422.1:p.Ser242Phe
CA370198078
NM_005431.2:c.725C>T