Canonical Allele Identifier: PA2828013661
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala61Thr
CA006037
NM_001354903.2:c.181G>A