Canonical Allele Identifier: PA2828022331
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236603

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser1276Phe
CA10582316
NM_001354906.2:c.3827C>T