Canonical Allele Identifier: PA2829392027
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 246163
ClinVar RCV Id: RCV000235241 RCV000567552 RCV000648254 RCV002500834
ClinVar Variation Id: 818633
ClinVar RCV Id: RCV001010407 RCV001860636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Val41Leu
CA10584579
NM_002876.4:c.121G>C
CA400337598
NM_002876.4:c.121G>T