Canonical Allele Identifier: PA288623
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 128203
ClinVar RCV Id: RCV000116172 RCV000123370 RCV000411171 RCV000590726 RCV002307397 RCV002483192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Thr5Met
CA288621
NM_058216.3:c.14C>T