Canonical Allele Identifier: PA2828019611
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1730223
ClinVar RCV Id: RCV002326403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asn1007Ile
CA16028622
NM_001354903.2:c.3020A>T