Canonical Allele Identifier: PA2829391442
Gene: RAD51 HGNC NCBI

Linked Data

ClinVar Variation Id: 1740068
ClinVar RCV Id: RCV002333487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002866.2:p.Leu146Phe
CA391753217
NM_002875.5:c.436C>T