Canonical Allele Identifier: PA2828028301
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 229765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Pro2188Leu
CA10578443
NM_001354906.2:c.6563C>T