Canonical Allele Identifier: PA2825800129
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 420660
ClinVar RCV Id: RCV000481968 RCV001865452 RCV002436538 RCV003482146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136043.1:p.Met1Arg