Canonical Allele Identifier: PA2830246091
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_598332.1:p.Gly213Ser
CA287999
NM_133629.3:c.637G>A