Canonical Allele Identifier: PA2828012115
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2406Thr
CA16037620
NM_001354902.2:c.7216T>A