Canonical Allele Identifier: PA2828001615
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp1042Glu
CA16028782
NM_001354902.2:c.3126T>A
CA16028783
NM_001354902.2:c.3126T>G