Canonical Allele Identifier: PA2827949552
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 946413

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser296Asn
CA16023257
NM_001354896.2:c.887G>A