Canonical Allele Identifier: PA2825970336
Gene: RAD51 HGNC NCBI

Linked Data

ClinVar Variation Id: 1740771
ClinVar RCV Id: RCV002328422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157741.1:p.Asp150Tyr
CA391753258
NM_001164269.2:c.448G>T