Canonical Allele Identifier: PA2829392046
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1719748
ClinVar RCV Id: RCV002303945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Ser44Tyr
CA400337719
NM_002876.4:c.131C>A