Canonical Allele Identifier: PA645460086
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 232301
ClinVar RCV Id: RCV000223596 RCV000586089 RCV000648262 RCV002247658 RCV003469054
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Ser29Phe
CA10580722
NM_058216.3:c.86C>T