Canonical Allele Identifier: PA2580176497
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1775799
ClinVar RCV Id: RCV002398316

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Thr529Asn
CA374104612
NM_001243743.2:c.1586C>A