Canonical Allele Identifier: PA2827977453
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236603

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser1531Phe
CA10582316
NM_001354899.2:c.4592C>T