Canonical Allele Identifier: PA2573067767
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1300396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Asn164Thr
CA196885560
NM_001243744.2:c.491A>C