Canonical Allele Identifier: PA915996834
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 646190
ClinVar RCV Id: RCV000800424
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005422.1:p.Ser103Arg
CA370198985
NM_005431.2:c.309C>G
CA370198986
NM_005431.2:c.309C>A
CA370198990
NM_005431.2:c.307A>C