Canonical Allele Identifier: PA645456642
Gene: RAD50 HGNC NCBI

Linked Data

ClinVar Variation Id: 408392
ClinVar RCV Id: RCV000464040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005723.2:p.Ser128Arg
CA16611942
NM_005732.3:c.384T>G
CA360933373
NM_005732.3:c.382A>C
CA360933419
NM_005732.3:c.384T>A