Canonical Allele Identifier: PA916006595
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 234312
ClinVar RCV Id: RCV000222127 RCV001011947 RCV000799605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Thr503Met
CA5137322
NM_001243743.2:c.1508C>T