Canonical Allele Identifier: PA338968
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 216807
ClinVar RCV Id: RCV000199916 RCV000220144 RCV000679802 RCV000765377 RCV001358631 RCV001798674 RCV004020476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Lys235Asn
CA338966
NM_058216.3:c.705G>T
CA400350187
NM_058216.3:c.705G>C