Canonical Allele Identifier: PA658668906
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 472611
ClinVar RCV Id: RCV000542552 RCV002330951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002869.3:p.Gln160Glu
CA399089143
NM_002878.4:c.478C>G