Canonical Allele Identifier: PA2829391450
Gene: RAD51 HGNC NCBI

Linked Data

ClinVar Variation Id: 1740771
ClinVar RCV Id: RCV002328422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002866.2:p.Asp149Tyr
CA391753258
NM_002875.5:c.445G>T