Canonical Allele Identifier: PA2826329825
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1300396
ClinVar RCV Id: RCV001732365 RCV002343807 RCV002488492 RCV002539805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Asn164Thr
CA196885560
NM_001243743.2:c.491A>C