Canonical Allele Identifier: PA2827998246
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1757245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Met2314Ile
CA16036834
NM_001354901.2:c.6942G>A
CA16036835
NM_001354901.2:c.6942G>C
CA16036836
NM_001354901.2:c.6942G>T