Canonical Allele Identifier: PA2825637556
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gly249Glu
CA049608
NM_001127511.3:c.746G>A