Allele Registry

Canonical Allele Identifier: PA2825055951

Gene: FANCC HGNC NCBI

ClinVar Variation Id: 1744384

HGVS (amino-acid)	Matching Registered Transcripts
NP_000127.2:p.Phe397Leu	CA374107506 NM_000136.3:c.1191C>G CA374107507 NM_000136.3:c.1191C>A CA374107512 NM_000136.3:c.1189T>C