Canonical Allele Identifier: PA2828032042
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Gly242Glu
CA049608
NM_001354904.2:c.725G>A