Canonical Allele Identifier: PA2829392221
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 241767
ClinVar RCV Id: RCV000231279 RCV000236604 RCV000568017 RCV001354084 RCV002487092 RCV003463687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Thr78Ile
CA8677187
NM_002876.4:c.233C>T