Canonical Allele Identifier: PA165930
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 141609
ClinVar RCV Id: RCV000130201 RCV000483361 RCV000649709 RCV001196273 RCV001818310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002869.3:p.Ser144Phe
CA165928
NM_002878.4:c.431C>T