Canonical Allele Identifier: PA2827985071
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser1085Ile
CA035157
NM_001354900.2:c.3254G>T