Canonical Allele Identifier: PA2828029687
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489502

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr2396Ile
CA16038783
NM_001354906.2:c.7187C>T