Allele Registry

Canonical Allele Identifier: PA2826331096

Gene: FANCC HGNC NCBI

ClinVar Allele:

407749

ClinVar RCV:

RCV000484866

RCV000988211

RCV001017686

RCV001243848

RCV003409651

ClinVar Variation:

418188

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230672.1:p.Ser280Leu	CA5137627 NM_001243743.2:c.839C>T