Canonical Allele Identifier: PA2828027971
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr2139Ala
CA012961
NM_001354906.2:c.6415A>G