Canonical Allele Identifier: PA2830246048
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_598332.1:p.Ile199Met
CA10649026
NM_133629.3:c.597T>G