Canonical Allele Identifier: PA2826329827
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 409660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Asn170Ser
CA5137718
NM_001243743.2:c.509A>G