Canonical Allele Identifier: PA2827989199
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1506415
ClinVar RCV Id: RCV003773379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Leu2337Ile
CA16036865
NM_001354900.2:c.7009C>A