Canonical Allele Identifier: PA2828011940
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 658256

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2368Cys
CA16037401
NM_001354902.2:c.7103C>G