Canonical Allele Identifier: PA2827998465
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485161
ClinVar RCV Id: RCV000576085 RCV001858358 RCV003459377 RCV004001108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg2380His
CA16037262
NM_001354901.2:c.7139G>A