Canonical Allele Identifier: PA2827973379
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1368868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr269Ile
CA16023266
NM_001354899.2:c.806C>T