ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA190617
Gene: RAD51C
HGNC
NCBI
Linked Data
ClinVar Variation Id:
184967
ClinVar RCV Id:
RCV000164316
RCV001850293
RCV002492656
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_478123.1:p.Ile177Val
CA190615
NM_058216.3:c.529A>G