Canonical Allele Identifier: PA2826330421
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 456161
ClinVar RCV Id: RCV000551381 RCV002323916 RCV003478126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Leu110Pro
CA5137779
NM_001243743.2:c.329T>C