Canonical Allele Identifier: PA2828051901
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2988779
ClinVar RCV Id: RCV003846946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser236Asn
CA16023250
NM_001354905.2:c.707G>A