Canonical Allele Identifier: PA2580176618
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1729701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Lys109Asn
CA374339221
NM_001243744.2:c.327A>T
CA374339222
NM_001243744.2:c.327A>C