Allele Registry

Canonical Allele Identifier: PA916007097

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000549299

RCV002384041

ClinVar Variation:

456149

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230673.1:p.Thr344Ala	CA374108173 NM_001243744.2:c.1030A>G