Canonical Allele Identifier: PA300476
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182996
ClinVar RCV Id: RCV000765951 RCV000767011 RCV001024734 RCV001818361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005422.1:p.Met199Thr
CA300475
NM_005431.2:c.596T>C