Allele Registry

Canonical Allele Identifier: PA2826329917

Gene: FANCC HGNC NCBI

ClinVar Allele:

132986

ClinVar RCV:

RCV000115339

RCV000630863

RCV001009634

RCV001030468

ClinVar Variation:

127529

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230672.1:p.Arg334Gln	CA287178 NM_001243743.2:c.1001G>A