Canonical Allele Identifier: PA167406
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 142102
ClinVar RCV Id: RCV000130934 RCV000204202 RCV000590382 RCV000722123 RCV001798446 RCV001270344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002869.3:p.Ser207Leu
CA167404
NM_002878.4:c.620C>T