Canonical Allele Identifier: PA2741865210
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2757713
ClinVar RCV Id: RCV003536915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr986Ile
CA16028647
NM_001354904.2:c.2957C>T