Canonical Allele Identifier: PA2828011842
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr2331Ala
CA012961
NM_001354902.2:c.6991A>G