Canonical Allele Identifier: PA916006842
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 456163
ClinVar RCV Id: RCV000550475 RCV001821481 RCV000566915 RCV001276460 RCV002254930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Tyr146del
CA5137747
NM_001243744.2:c.436_438del