Canonical Allele Identifier: PA2827980432
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 229765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro2443Leu
CA10578443
NM_001354899.2:c.7328C>T