Canonical Allele Identifier: PA2826330027
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 127538
ClinVar RCV Id: RCV000233348 RCV000567825 RCV000656849 RCV000709097 RCV001358189 RCV001818266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Cys10Tyr
CA287205
NM_001243743.2:c.29G>A