Allele Registry

Canonical Allele Identifier: PA2826330067

Gene: FANCC HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

138040

ClinVar RCV:

RCV000120974

RCV000513630

RCV000573438

RCV000988227

RCV001083879

RCV001168031

RCV001357504

RCV003891642

ClinVar Variation:

134301

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230672.1:p.Ser26Phe	CA159399 NM_001243743.2:c.77C>T