Canonical Allele Identifier: PA2827949960
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala440Thr
CA16024191
NM_001354896.2:c.1318G>A