Canonical Allele Identifier: PA645402342
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr2623Ala
CA16038426
NM_001127510.3:c.7867A>G