Canonical Allele Identifier: PA2829391963
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 482167
ClinVar RCV Id: RCV000575411 RCV001858214
ClinVar Variation Id: 1762833
ClinVar RCV Id: RCV002430344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Val28Leu
CA400337090
NM_002876.4:c.82G>C
CA400337095
NM_002876.4:c.82G>T