Canonical Allele Identifier: PA2826331774
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1420331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Met443Ile
CA5137399
NM_001243743.2:c.1329G>A
CA374107216
NM_001243743.2:c.1329G>T
CA374107217
NM_001243743.2:c.1329G>C