Canonical Allele Identifier: PA916040914
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp2051Glu
CA010908
NM_001354896.2:c.6153C>G
CA16034682
NM_001354896.2:c.6153C>A