Canonical Allele Identifier: PA2825644718
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr2608Ala
CA049327
NM_001127511.3:c.7822A>G