Canonical Allele Identifier: PA645402709
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_000127.2:p.His452_Leu453delinsArgHis
CA16618876
NM_000136.3:c.1355_1358delinsGCCA