Canonical Allele Identifier: PA2827998225
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 571390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr2308Ala
CA046911
NM_001354901.2:c.6922A>G