Canonical Allele Identifier: PA2828044209
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1171348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr1821Ile
CA16034105
NM_001354904.2:c.5462C>T