Canonical Allele Identifier: PA645460274
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 421729
ClinVar RCV Id: RCV000479624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Val239Met
CA16620500
NM_058216.3:c.715G>A