Canonical Allele Identifier: PA891852506
Gene: RAD50 HGNC NCBI

Linked Data

ClinVar Variation Id: 577614
ClinVar RCV Id: RCV000700415
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005723.2:p.Phe111Leu
CA360931278
NM_005732.3:c.331T>C
CA360931302
NM_005732.3:c.333T>A
CA360931306
NM_005732.3:c.333T>G