Canonical Allele Identifier: PA2825644675
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr2593Lys
CA049276
NM_001127511.3:c.7778C>A