Canonical Allele Identifier: PA2825056034
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 840072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Arg436Lys
CA196543203
NM_000136.3:c.1307G>A