Canonical Allele Identifier: PA2826330011
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2143434
ClinVar RCV Id: RCV003062709

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Asp7Glu
CA374340510
NM_001243743.2:c.21T>G
CA374340511
NM_001243743.2:c.21T>A