Canonical Allele Identifier: PA2826330505
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1737014
ClinVar RCV Id: RCV002357848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Phe134Leu
CA374338806
NM_001243743.2:c.402C>G
CA374338807
NM_001243743.2:c.402C>A
CA374338812
NM_001243743.2:c.400T>C