Allele Registry

Canonical Allele Identifier: PA916007083

Gene: FANCC HGNC NCBI

ClinVar Allele:

212681

ClinVar RCV:

RCV000195976

RCV000486496

RCV001009657

RCV001354801

RCV001818484

ClinVar Variation:

216279

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230673.1:p.Arg334Trp	CA336089 NM_001243744.2:c.1000C>T