Canonical Allele Identifier: PA2828046184
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr2117Ala
CA045904
NM_001354904.2:c.6349A>G