Canonical Allele Identifier: PA916006632
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 127535
ClinVar RCV Id: RCV000115345 RCV000228424 RCV001012346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Arg535His
CA287196
NM_001243743.2:c.1604G>A