Canonical Allele Identifier: PA337033
Gene: RAD50 HGNC NCBI

Linked Data

ClinVar Variation Id: 216616
ClinVar RCV Id: RCV000197198

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005723.2:p.Phe388Leu
CA337032
NM_005732.3:c.1164C>G
CA127243896
NM_005732.3:c.1162T>C
CA360942732
NM_005732.3:c.1164C>A