Canonical Allele Identifier: PA2828024779
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1477212
ClinVar RCV Id: RCV003773118
ClinVar Variation Id: 2452715
ClinVar RCV Id: RCV003177489

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asp1665Glu
CA16034112
NM_001354906.2:c.4995T>A
CA16034113
NM_001354906.2:c.4995T>G