Canonical Allele Identifier: PA2827999730
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asp2762Gly
CA050869
NM_001354901.2:c.8285A>G