Canonical Allele Identifier: PA333278
Gene: RAD50 HGNC NCBI

Linked Data

ClinVar Variation Id: 142598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005723.2:p.Arg1166Trp
CA333277
NM_005732.3:c.3496C>T