Canonical Allele Identifier: PA2499295671
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1009535
ClinVar RCV Id: RCV001307041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Ile208Ser
CA400349417
NM_058216.3:c.623T>G