Canonical Allele Identifier: PA2828028566
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2561155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2391Phe
CA16037595
NM_001354903.2:c.7172C>T