Canonical Allele Identifier: PA916039760
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Tyr755His
CA031174
NM_001354896.2:c.2263T>C