Canonical Allele Identifier: PA1139694208
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 951963
ClinVar RCV Id: RCV001223977 RCV001358076 RCV002402696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Leu546Val
CA374104339
NM_001243743.2:c.1636C>G