Canonical Allele Identifier: PA2828016438
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Val508Ile
CA006055
NM_001354903.2:c.1522G>A