Canonical Allele Identifier: PA2829392561
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 182835
ClinVar RCV Id: RCV000160923 RCV000221514 RCV000467500 RCV000763014 RCV002307418 RCV003467269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Trp135_Ter136insGlnAsnLysValPheSerPhe
CA299885
NM_002876.4:c.406T>C