Canonical Allele Identifier: PA2827948933
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Leu93His
CA10578288
NM_001354896.2:c.278T>A