Canonical Allele Identifier: PA2825644498
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760034
ClinVar RCV Id: RCV002396452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.His2536Asn
CA16037972
NM_001127511.3:c.7606C>A