Canonical Allele Identifier: PA2828001233
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala837Thr
CA007787
NM_001354902.2:c.2509G>A