Canonical Allele Identifier: PA2826330028
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 216287
ClinVar RCV Id: RCV000200177 RCV000218236 RCV000709098 RCV001016913 RCV001818485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Cys10Gly
CA339141
NM_001243743.2:c.28T>G