Canonical Allele Identifier: PA891845116
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 584741
ClinVar RCV Id: RCV000709092 RCV001247684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Leu138Arg
CA374338780
NM_000136.3:c.413T>G