Canonical Allele Identifier: PA2825643924
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 571390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr2349Ala
CA046911
NM_001127511.3:c.7045A>G