Canonical Allele Identifier: PA2580176662
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2145928
ClinVar RCV Id: RCV003065285 RCV003294435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Thr171Pro
CA374338560
NM_001243744.2:c.511A>C