Canonical Allele Identifier: PA2826330059
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 826244
ClinVar RCV Id: RCV001025004 RCV002551910 RCV001276599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Val21Leu
CA5137842
NM_001243743.2:c.61G>C
CA374340419
NM_001243743.2:c.61G>T