Canonical Allele Identifier: PA2828008818
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr1354Ile
CA009453
NM_001354902.2:c.4061C>T