Canonical Allele Identifier: PA916006528
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 419059
ClinVar RCV Id: RCV000485198 RCV002506162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.His452_Leu453delinsArgHis
CA16618876
NM_001243743.2:c.1355_1358delinsGCCA