Allele Registry

Canonical Allele Identifier: PA916006565

Gene: FANCC HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

138038

3385206

ClinVar RCV:

RCV000120972

RCV000205771

RCV001011455

RCV001310662

RCV001509574

RCV004520513

ClinVar Variation:

134299

3230362

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230672.1:p.Gly472Arg	CA332152 NM_001243743.2:c.1414G>A CA374106050 NM_001243743.2:c.1414G>C