Canonical Allele Identifier: PA168557
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 142510
ClinVar RCV Id: RCV000131660 RCV000701475 RCV001762314
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Pro21Leu
CA168555
NM_058216.3:c.62C>T