Canonical Allele Identifier: PA2827981299
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala2702Ser
CA16039107
NM_001354899.2:c.8104G>T