Canonical Allele Identifier: PA2827954070
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Val1143Ala
CA008333
NM_001354896.2:c.3428T>C