Canonical Allele Identifier: PA2828021596
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr1162Ala
CA009444
NM_001354906.2:c.3484A>G