Canonical Allele Identifier: PA2828005767
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1714181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr537Ile
CA029849
NM_001354902.2:c.1610C>T