Canonical Allele Identifier: PA163969
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 140940
ClinVar RCV Id: RCV000129215 RCV000167882 RCV000409379 RCV000588471 RCV001778747 RCV001798436 RCV002509232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Glu45Gly
CA163967
NM_058216.3:c.134A>G