Canonical Allele Identifier: PA1139760942
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 935624
ClinVar RCV Id: RCV001204262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Glu303Asp
CA400361288
NM_058216.3:c.909A>C
CA400361290
NM_058216.3:c.909A>T