Canonical Allele Identifier: PA2825635190
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760034
ClinVar RCV Id: RCV002396452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.His2554Asn
CA16037972
NM_001127510.3:c.7660C>A