Canonical Allele Identifier: PA916006637
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 127536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Leu536Pro
CA287199
NM_001243743.2:c.1607T>C