Canonical Allele Identifier: PA2828013309
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3069477
ClinVar RCV Id: RCV004008021

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Val2491Ile
CA16038596
NM_001354905.2:c.7471G>A