Canonical Allele Identifier: PA2827999088
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1489600
ClinVar RCV Id: RCV003773222
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2568del
CA2573138677
NM_001354901.2:c.7702_7704del