Canonical Allele Identifier: PA2827964077
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470104

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp231Glu
CA16023011
NM_001354898.2:c.693T>A
CA16023012
NM_001354898.2:c.693T>G