Canonical Allele Identifier: PA2828027779
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 188173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2115Phe
CA012909
NM_001354906.2:c.6344C>T