ClinGen Allele Registry
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Canonical Allele Identifier:
PA331907
Gene: RAD51C
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
133667
ClinVar RCV:
RCV000116179
RCV000206074
RCV000411451
RCV000585995
RCV000765378
RCV000778506
RCV001195025
RCV001356788
RCV001778711
RCV001798365
ClinVar Variation:
128210
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_478123.1:p.Leu262Val
CA331905
NM_058216.3:c.784T>G