Canonical Allele Identifier: PA2828054932
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 188207
ClinVar RCV Id: RCV000168132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser746Ala
CA007751
NM_001354905.2:c.2236T>G