Canonical Allele Identifier: PA2828016940
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Val603Ile
CA007204
NM_001354903.2:c.1807G>A