Canonical Allele Identifier: PA916041804
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala2813Thr
CA015437
NM_001354896.2:c.8437G>A