Canonical Allele Identifier: PA2826331567
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1744384
ClinVar RCV Id: RCV002342779

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Phe397Leu
CA374107506
NM_001243743.2:c.1191C>G
CA374107507
NM_001243743.2:c.1191C>A
CA374107512
NM_001243743.2:c.1189T>C