Canonical Allele Identifier: PA2741997065
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 2625141
ClinVar RCV Id: RCV003379900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Cys176Ser
CA400345158
NM_058216.3:c.526T>A
CA400345165
NM_058216.3:c.527G>C