ClinGen Allele Registry
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Canonical Allele Identifier:
PA288626
Gene: RAD51C
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000116175
RCV000199007
RCV000412269
RCV000588889
RCV001358061
RCV002267859
RCV003492509
RCV004556053
ClinVar Variation:
128206
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_478123.1:p.Val169Ala
CA288624
NM_058216.3:c.506T>C