Canonical Allele Identifier: PA916055864
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 662201
ClinVar RCV Id: RCV000819800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Asn263Ser
CA292059449
NM_058216.3:c.788A>G