Canonical Allele Identifier: PA2573067766
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1329751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Val154Gly
CA374338666
NM_001243744.2:c.461T>G