Canonical Allele Identifier: PA2829391932
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1375255
ClinVar RCV Id: RCV001879579
ClinVar Variation Id: 3228957
ClinVar RCV Id: RCV004522584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Val23Leu
CA400336845
NM_002876.4:c.67G>T
CA400336854
NM_002876.4:c.67G>C