Canonical Allele Identifier: PA2828049019
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3069477
ClinVar RCV Id: RCV004008021

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Val2525Ile
CA16038596
NM_001354904.2:c.7573G>A