Canonical Allele Identifier: PA131078
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 21030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Val1822Asp
CA010422
NM_001127510.3:c.5465T>A