Canonical Allele Identifier: PA2828011700
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr2288Pro
CA16036870
NM_001354902.2:c.6862A>C