Canonical Allele Identifier: PA2828002076
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala1267Thr
CA008897
NM_001354902.2:c.3799G>A