Canonical Allele Identifier: PA165189
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 141353
ClinVar RCV Id: RCV000129840 RCV000648258 RCV001818306 RCV003105794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Lys188Met
CA165187
NM_058216.3:c.563A>T