Canonical Allele Identifier: PA338915
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 216283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Met456Ile
CA338913
NM_000136.3:c.1368G>T
CA374106221
NM_000136.3:c.1368G>C
CA374106222
NM_000136.3:c.1368G>A