Canonical Allele Identifier: PA2828047848
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2371Thr
CA16037620
NM_001354904.2:c.7111T>A