Canonical Allele Identifier: PA288001
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 127898
ClinVar RCV Id: RCV000115824 RCV000571425 RCV000709426 RCV000554021 RCV000656968 RCV003415892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002869.3:p.Gly325Ser
CA287999
NM_002878.4:c.973G>A