Canonical Allele Identifier: PA2827951393
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.His1228Leu
CA035977
NM_001354896.2:c.3683A>T