Canonical Allele Identifier: PA2827981295
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1318535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala2702Asp
CA16039108
NM_001354899.2:c.8105C>A