Canonical Allele Identifier: PA2573186618
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1389407
ClinVar RCV Id: RCV001917359 RCV002397850
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Lys552Gln
CA374104264
NM_001243743.2:c.1654A>C