Canonical Allele Identifier: PA1139694859
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 485542
ClinVar RCV Id: RCV000565785 RCV001853768 RCV001273983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Tyr430del
CA589580888
NM_001243744.2:c.1288_1290del