Canonical Allele Identifier: PA2827987213
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 423629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gly1726Asp
CA16032918
NM_001354900.2:c.5177G>A