Allele Registry

Canonical Allele Identifier: PA916006564

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000487102

RCV000988195

RCV001011411

RCV001247526

RCV001328458

RCV002481503

ClinVar Variation:

419042

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230672.1:p.Thr469Met	CA5137337 NM_001243743.2:c.1406C>T