Canonical Allele Identifier: PA2827949582
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1439196

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser306Ile
CA16023319
NM_001354896.2:c.917G>T