Canonical Allele Identifier: PA2828022476
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236603

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser1458Phe
CA10582316
NM_001354903.2:c.4373C>T