Canonical Allele Identifier: PA2827968635
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1058153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly1649Glu
CA16032317
NM_001354898.2:c.4946G>A