Canonical Allele Identifier: PA645400847
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 419583
ClinVar RCV Id: RCV000482075 RCV001276467 RCV002350058 RCV002525805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Tyr12Cys
CA5137846
NM_000136.3:c.35A>G