Canonical Allele Identifier: PA2825629650
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 921338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp1016Asn
CA16028000
NM_001127510.3:c.3046G>A