Canonical Allele Identifier: PA2827971718
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr2586Ile
CA014100
NM_001354898.2:c.7757C>T