Canonical Allele Identifier: PA2580176641
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2446649
ClinVar RCV Id: RCV003159479

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Ile143Met
CA5137749
NM_001243744.2:c.429A>G