Canonical Allele Identifier: PA2827977160
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala1447Val
CA009538
NM_001354899.2:c.4340C>T