Canonical Allele Identifier: PA2828041084
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236603

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser1433Phe
CA10582316
NM_001354904.2:c.4298C>T