Canonical Allele Identifier: PA2825024005
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr2379Pro
CA16036870
NM_000038.6:c.7135A>C