Canonical Allele Identifier: PA130239
Gene: RAD50 HGNC NCBI

Linked Data

ClinVar Variation Id: 37383
ClinVar RCV Id: RCV000030964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005723.2:p.His862Arg
CA130238
NM_005732.3:c.2585A>G