ClinGen Allele Registry
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Canonical Allele Identifier:
PA299866
Gene: RAD51C
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
180917
ClinVar RCV:
RCV000160916
RCV000168412
RCV000234871
RCV000663073
RCV000781789
RCV001257495
ClinVar Variation:
182828
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_478123.1:p.Arg249His
CA299864
NM_058216.3:c.746G>A