Canonical Allele Identifier: PA2826331096
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 418188
ClinVar RCV Id: RCV000484866 RCV000988211 RCV001017686 RCV001243848 RCV003409651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ser280Leu
CA5137627
NM_001243743.2:c.839C>T