Canonical Allele Identifier: PA916006558
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 216283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Met456Ile
CA338913
NM_001243743.2:c.1368G>T
CA374106221
NM_001243743.2:c.1368G>C
CA374106222
NM_001243743.2:c.1368G>A