Canonical Allele Identifier: PA2827998267
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr2320Pro
CA16036870
NM_001354901.2:c.6958A>C