Canonical Allele Identifier: PA2828047670
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 229765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro2345Leu
CA10578443
NM_001354904.2:c.7034C>T