Canonical Allele Identifier: PA915979709
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 230736
ClinVar RCV Id: RCV000218087 RCV000523045 RCV000819998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136043.1:p.Glu338Lys
CA10580438
NM_001142571.2:c.1012G>A