Canonical Allele Identifier: PA2827962625
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr2636Ile
CA014137
NM_001354897.2:c.7907C>T