Canonical Allele Identifier: PA2580176495
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1775371
ClinVar RCV Id: RCV002405524

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ile522Met
CA374104712
NM_001243743.2:c.1566C>G