Canonical Allele Identifier: PA2828055296
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 921338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asp856Asn
CA16028000
NM_001354905.2:c.2566G>A