Canonical Allele Identifier: PA2826329821
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 418577
ClinVar RCV Id: RCV000485063 RCV001066884 RCV002341128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ala158Val
CA5137724
NM_001243743.2:c.473C>T