Canonical Allele Identifier: PA658671369
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 480512
ClinVar RCV Id: RCV000566985 RCV001219253
ClinVar Variation Id: 1467471
ClinVar RCV Id: RCV001993423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Thr365Ser
CA400366433
NM_058216.3:c.1093A>T
CA400366444
NM_058216.3:c.1094C>G