Canonical Allele Identifier: PA2573186674
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1481043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Ile114Val
CA374339172
NM_001243744.2:c.340A>G