Canonical Allele Identifier: PA168759
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 142585
ClinVar RCV Id: RCV000131788 RCV000232947 RCV000482155 RCV001270237 RCV003462023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Ser364Gly
CA168757
NM_058216.3:c.1090A>G