Canonical Allele Identifier: PA2499242470
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1049437
ClinVar RCV Id: RCV001355555 RCV002341742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Ala2Thr
CA374340545
NM_001243744.2:c.4G>A