Canonical Allele Identifier: PA916042066
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala71Thr
CA006037
NM_001354902.2:c.211G>A