Allele Registry

Canonical Allele Identifier: PA2826329925

Gene: FANCC HGNC NCBI

ClinVar Allele:

221841

ClinVar RCV:

RCV000206395

RCV000479585

RCV002426960

ClinVar Variation:

219624

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230672.1:p.Arg361Trp	CA350435 NM_001243743.2:c.1081C>T