Canonical Allele Identifier: PA2828046977
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1757245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Met2247Ile
CA16036834
NM_001354904.2:c.6741G>A
CA16036835
NM_001354904.2:c.6741G>C
CA16036836
NM_001354904.2:c.6741G>T