Canonical Allele Identifier: PA2828003367
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp1942Glu
CA010908
NM_001354902.2:c.5826C>G
CA16034682
NM_001354902.2:c.5826C>A