Canonical Allele Identifier: PA2827989159
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 571390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr2326Ala
CA046911
NM_001354900.2:c.6976A>G