Canonical Allele Identifier: PA916006613
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 819542

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.His520Gln
CA374104747
NM_001243743.2:c.1560C>G
CA374104749
NM_001243743.2:c.1560C>A