Canonical Allele Identifier: PA2828011764
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 188173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2307Phe
CA012909
NM_001354902.2:c.6920C>T