Canonical Allele Identifier: PA2573067744
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1338426
ClinVar RCV Id: RCV001817797
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Lys545del
CA2573053198
NM_001243743.2:c.1633_1635del