Canonical Allele Identifier: PA2827999082
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr2567Ser
CA16038447
NM_001354901.2:c.7699A>T
CA16038449
NM_001354901.2:c.7700C>G