Canonical Allele Identifier: PA2829391808
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 484753
ClinVar RCV Id: RCV000572971 RCV002526888 RCV003459372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Thr5Arg
CA8677119
NM_002876.4:c.14C>G