Canonical Allele Identifier: PA2828029392
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 350423

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr2352Ala
CA10622269
NM_001354906.2:c.7054A>G