Canonical Allele Identifier: PA2825634871
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1757245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Met2373Ile
CA16036834
NM_001127510.3:c.7119G>A
CA16036835
NM_001127510.3:c.7119G>C
CA16036836
NM_001127510.3:c.7119G>T