Canonical Allele Identifier: PA916006612
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 449977
ClinVar RCV Id: RCV000523904 RCV000563212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ala516Phe
CA658657887
NM_001243743.2:c.1546_1547delinsTT