Canonical Allele Identifier: PA2827949563
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser299Thr
CA051068
NM_001354896.2:c.895T>A