Canonical Allele Identifier: PA165672
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 141519
ClinVar RCV Id: RCV000130084 RCV000255993 RCV000411407 RCV001357548 RCV001193713 RCV002508924 RCV003492595 RCV003483498 RCV003891666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002869.3:p.Arg266Cys
CA165670
NM_002878.4:c.796C>T