Canonical Allele Identifier: PA2826331080
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 219885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Phe275Leu
CA349095
NM_001243743.2:c.823T>C
CA374109205
NM_001243743.2:c.825T>G
CA374109206
NM_001243743.2:c.825T>A