Allele Registry

Canonical Allele Identifier: PA916006965

Gene: FANCC HGNC NCBI

ClinVar Allele:

221854

ClinVar RCV:

RCV000204753

RCV000482871

RCV001025655

ClinVar Variation:

220497

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230673.1:p.Ile227Val	CA348958 NM_001243744.2:c.679A>G