Canonical Allele Identifier: PA2827998217
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 854549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Met2305Ile
CA16036777
NM_001354901.2:c.6915G>A
CA16036778
NM_001354901.2:c.6915G>C
CA16036779
NM_001354901.2:c.6915G>T