Canonical Allele Identifier: PA2825970353
Gene: RAD51 HGNC NCBI

Linked Data

ClinVar Variation Id: 1743549
ClinVar RCV Id: RCV002330800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157741.1:p.Thr163Ala
CA391753443
NM_001164269.2:c.487A>G