Canonical Allele Identifier: PA2827992023
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1316460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ile387Leu
CA16024229
NM_001354901.2:c.1159A>C