Canonical Allele Identifier: PA2826332097
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 3230367
ClinVar RCV Id: RCV004520518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ile518Leu
CA374104789
NM_001243743.2:c.1552A>T
CA374104794
NM_001243743.2:c.1552A>C