Canonical Allele Identifier: PA645402671
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 418189
ClinVar RCV Id: RCV000478222 RCV000702767 RCV002413315 RCV001355099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Leu422Met
CA5137407
NM_000136.3:c.1264C>A