Canonical Allele Identifier: PA198119
Gene: RAD50 HGNC NCBI

Linked Data

ClinVar Variation Id: 187622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005723.2:p.Gln737Glu
CA198118
NM_005732.3:c.2209C>G