Canonical Allele Identifier: PA645461965
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 230594
ClinVar RCV Id: RCV000222465 RCV000555250 RCV001547298 RCV002229933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002869.3:p.Arg55Trp
CA8499638
NM_002878.4:c.163C>T