Canonical Allele Identifier: PA2828023899
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 21030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Val1539Asp
CA010422
NM_001354906.2:c.4616T>A