Canonical Allele Identifier: PA2827980082
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 571390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr2339Ala
CA046911
NM_001354899.2:c.7015A>G