Canonical Allele Identifier: PA916006565
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 134299
ClinVar RCV Id: RCV000205771 RCV000120972 RCV001011455 RCV001310662 RCV001509574
ClinVar Variation Id: 3230362
ClinVar RCV Id: RCV004520513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Gly472Arg
CA332152
NM_001243743.2:c.1414G>A
CA374106050
NM_001243743.2:c.1414G>C