Canonical Allele Identifier: PA2828023948
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 423629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gly1666Asp
CA16032918
NM_001354903.2:c.4997G>A