Canonical Allele Identifier: PA915979693
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 322623
ClinVar RCV Id: RCV000708751 RCV003642884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136043.1:p.Ile331Met
CA10649026
NM_001142571.2:c.993T>G