Canonical Allele Identifier: PA2827980938
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr2598Ser
CA16038447
NM_001354899.2:c.7792A>T
CA16038449
NM_001354899.2:c.7793C>G