Canonical Allele Identifier: PA2829391832
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 538779
ClinVar RCV Id: RCV000648251 RCV001013997 RCV001592805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Arg7Ser
CA400336232
NM_002876.4:c.19C>A