Allele Registry

Canonical Allele Identifier: PA2826329846

Gene: FANCC HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

138044

ClinVar RCV:

RCV000120978

RCV000124962

RCV000179716

RCV000667368

RCV000988215

RCV001083500

RCV001356570

ClinVar Variation:

134305

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230672.1:p.Asp195Val	CA247025 NM_001243743.2:c.584A>T