Canonical Allele Identifier: PA2829391972
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 480944
ClinVar RCV Id: RCV000574008 RCV000705597 RCV001770506 RCV003459310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Ala30Val
CA292047058
NM_002876.4:c.89C>T