Canonical Allele Identifier: PA2826329921
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 134295
ClinVar RCV Id: RCV000120968 RCV000766565 RCV001009799 RCV001300842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Asp355His
CA159384
NM_001243743.2:c.1063G>C