Canonical Allele Identifier: PA2828051553
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gly208Glu
CA049608
NM_001354905.2:c.623G>A