Allele Registry

Canonical Allele Identifier: PA916006994

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000160480

RCV000459016

RCV001027088

RCV001274477

ClinVar Variation:

182479

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230673.1:p.Cys268Ser	CA299166 NM_001243744.2:c.802T>A CA374109250 NM_001243744.2:c.803G>C