Canonical Allele Identifier: PA188886
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 184411
ClinVar RCV Id: RCV000163662 RCV000228544 RCV000479892 RCV001195006
ClinVar Variation Id: 926172
ClinVar RCV Id: RCV001188570 RCV003617911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Gly3Arg
CA188884
NM_058216.3:c.7G>A
CA400336093
NM_058216.3:c.7G>C