Canonical Allele Identifier: PA2827991923
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411392

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Glu363Lys
CA026951
NM_001354901.2:c.1087G>A