Canonical Allele Identifier: PA2828024297
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 21030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Val1721Asp
CA010422
NM_001354903.2:c.5162T>A