Canonical Allele Identifier: PA916006600
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 526356
ClinVar RCV Id: RCV000630877 RCV002387999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Trp506Cys
CA374105503
NM_001243743.2:c.1518G>T
CA374105504
NM_001243743.2:c.1518G>C