Canonical Allele Identifier: PA915979727
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 472633
ClinVar RCV Id: RCV000532608 RCV001185232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136043.1:p.Asp346Ala
CA399086041
NM_001142571.2:c.1037A>C