Canonical Allele Identifier: PA299208
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 182493
ClinVar RCV Id: RCV000160495 RCV000709096 RCV000988226 RCV002256090 RCV002372044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Glu43Lys
CA299206
NM_000136.3:c.127G>A