Canonical Allele Identifier: PA2573205788
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1692381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2596Pro
CA16038121
NM_001354896.2:c.7786T>C