Canonical Allele Identifier: PA916041144
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr2261Ala
CA045904
NM_001354896.2:c.6781A>G