Allele Registry

Canonical Allele Identifier: PA916007102

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000709084

RCV001017185

RCV001825407

RCV003492140

ClinVar Variation:

584738

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230673.1:p.Gln357Glu	CA5137482 NM_001243744.2:c.1069C>G