Canonical Allele Identifier: PA2828028380
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2367Ala
CA047997
NM_001354903.2:c.7099T>G