Canonical Allele Identifier: PA2827977895
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485156

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala1672Thr
CA16032477
NM_001354899.2:c.5014G>A