Canonical Allele Identifier: PA2828001314
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile892Thr
CA007931
NM_001354902.2:c.2675T>C