Canonical Allele Identifier: PA2828029287
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr2340Ala
CA16038426
NM_001354906.2:c.7018A>G