Canonical Allele Identifier: PA190533
Gene: RAD50 HGNC NCBI

Linked Data

ClinVar Variation Id: 184939
ClinVar RCV Id: RCV000164282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005723.2:p.Ser447Leu
CA190532
NM_005732.3:c.1340C>T