Canonical Allele Identifier: PA2828008901
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1171348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr1787Ile
CA16034105
NM_001354905.2:c.5360C>T