Canonical Allele Identifier: PA2826330578
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1741882
ClinVar RCV Id: RCV002342449 RCV003102607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Val154Leu
CA374338670
NM_001243743.2:c.460G>C