Canonical Allele Identifier: PA334229
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 188173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2398Phe
CA012909
NM_001127510.3:c.7193C>T