Canonical Allele Identifier: PA2825643916
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 854549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Met2346Ile
CA16036777
NM_001127511.3:c.7038G>A
CA16036778
NM_001127511.3:c.7038G>C
CA16036779
NM_001127511.3:c.7038G>T