Canonical Allele Identifier: PA2828029408
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr2522Ala
CA16038426
NM_001354903.2:c.7564A>G