Allele Registry

Canonical Allele Identifier: PA916007122

Gene: FANCC HGNC NCBI

ClinVar Allele:

231727

ClinVar RCV:

RCV000218892

RCV001828093

RCV002450653

ClinVar Variation:

234807

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230673.1:p.Gln382Glu	CA5137453 NM_001243744.2:c.1144C>G