Canonical Allele Identifier: PA2825055710
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 648819
ClinVar RCV Id: RCV000803626 RCV002440697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ser280Pro
CA374109177
NM_000136.3:c.838T>C