Canonical Allele Identifier: PA1139760762
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 958054
ClinVar RCV Id: RCV001231143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.His250Asp
CA400353538
NM_058216.3:c.748C>G