Canonical Allele Identifier: PA2828014800
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220329

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala239Pro
CA047113
NM_001354903.2:c.715G>C