Canonical Allele Identifier: PA2828011651
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 854549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Met2273Ile
CA16036777
NM_001354902.2:c.6819G>A
CA16036778
NM_001354902.2:c.6819G>C
CA16036779
NM_001354902.2:c.6819G>T