Canonical Allele Identifier: PA2828029489
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 350423

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr2534Ala
CA10622269
NM_001354903.2:c.7600A>G