Allele Registry

Canonical Allele Identifier: PA2826329931

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000485470

RCV000570574

RCV000630858

RCV001274615

RCV002222522

ClinVar Variation:

418852

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230672.1:p.Ala415Val	CA16618879 NM_001243743.2:c.1244C>T