Canonical Allele Identifier: PA2827989202
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr2338Pro
CA16036870
NM_001354900.2:c.7012A>C