Canonical Allele Identifier: PA2828012464
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr2520Lys
CA049276
NM_001354902.2:c.7559C>A