Allele Registry

Canonical Allele Identifier: PA916006641

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000567655

RCV000630828

RCV002293461

ClinVar Variation:

485551

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230672.1:p.Pro541Leu	CA374104406 NM_001243743.2:c.1622C>T