Canonical Allele Identifier: PA2827987001
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 574199

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser1666Pro
CA16032519
NM_001354900.2:c.4996T>C