Canonical Allele Identifier: PA2828030514
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala2677Ser
CA014561
NM_001354903.2:c.8029G>T