Canonical Allele Identifier: PA332154
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_000127.2:p.Gly472Arg
CA332152
NM_000136.3:c.1414G>A
CA374106050
NM_000136.3:c.1414G>C