Canonical Allele Identifier: PA1139741849
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 960729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2593Pro
CA16038103
NM_001354896.2:c.7777T>C