Canonical Allele Identifier: PA916006611
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 367609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Thr515Ser
CA5137299
NM_001243743.2:c.1544C>G
CA374104833
NM_001243743.2:c.1543A>T