Canonical Allele Identifier: PA2825055331
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1481043
ClinVar RCV Id: RCV002000441 RCV002331563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ile114Val
CA374339172
NM_000136.3:c.340A>G