Canonical Allele Identifier: PA2827973370
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2988779
ClinVar RCV Id: RCV003846946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser267Asn
CA16023250
NM_001354899.2:c.800G>A