Allele Registry

Canonical Allele Identifier: PA2826330479

Gene: FANCC HGNC NCBI

ClinVar Allele:

407764

ClinVar RCV:

RCV000482048

RCV001835817

RCV003168961

ClinVar Variation:

421810

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230672.1:p.Val117Ile	CA5137757 NM_001243743.2:c.349G>A