Canonical Allele Identifier: PA2825056206
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1204056
ClinVar RCV Id: RCV001570304 RCV001827499 RCV002405252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ile523Val
CA374104708
NM_000136.3:c.1567A>G