Canonical Allele Identifier: PA916067661
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 410557
ClinVar RCV Id: RCV000473688 RCV000568530 RCV000709459 RCV000781799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598332.1:p.Thr27Lys
CA16615737
NM_133629.3:c.80C>A