Canonical Allele Identifier: PA2825055393
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2446649
ClinVar RCV Id: RCV003159479

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ile143Met
CA5137749
NM_000136.3:c.429A>G