Canonical Allele Identifier: PA2825056009
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2462821
ClinVar RCV Id: RCV003174737
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ala427Thr
CA374107323
NM_000136.3:c.1279G>A