Canonical Allele Identifier: PA1139708392
Gene: RAD50 HGNC NCBI

Linked Data

ClinVar Variation Id: 856201
ClinVar RCV Id: RCV001061607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005723.2:p.Asp137Tyr
CA360933694
NM_005732.3:c.409G>T