Canonical Allele Identifier: PA2825800881
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_001136043.1:p.Ser227Leu
CA167404
NM_001142571.2:c.680C>T