Canonical Allele Identifier: PA2827980793
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 801041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2552Ala
CA16038136
NM_001354899.2:c.7654T>G