Canonical Allele Identifier: PA916041347
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 188173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2416Phe
CA012909
NM_001354896.2:c.7247C>T