Canonical Allele Identifier: PA916006585
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 12050
ClinVar RCV Id: RCV000012830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Leu496Arg
CA256207
NM_001243743.2:c.1487T>G