Canonical Allele Identifier: PA2826329805
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1730284
ClinVar RCV Id: RCV002326460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Asn111Ser
CA5137778
NM_001243743.2:c.332A>G