Canonical Allele Identifier: PA2827961764
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 854549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Met2374Ile
CA16036777
NM_001354897.2:c.7122G>A
CA16036778
NM_001354897.2:c.7122G>C
CA16036779
NM_001354897.2:c.7122G>T