Canonical Allele Identifier: PA2826329870
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1014542
ClinVar RCV Id: RCV001313289 RCV002384390 RCV002493637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Arg245Gln
CA196562568
NM_001243743.2:c.734G>A