Canonical Allele Identifier: PA2827984610
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile942Thr
CA007931
NM_001354900.2:c.2825T>C