Canonical Allele Identifier: PA300478
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182997
ClinVar RCV Id: RCV000161109 RCV000726016 RCV000988015 RCV001024935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005422.1:p.Ser205Ala
CA300477
NM_005431.2:c.613T>G