Canonical Allele Identifier: PA2827992162
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1051609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asp432Glu
CA16024530
NM_001354901.2:c.1296C>A
CA16024531
NM_001354901.2:c.1296C>G