Canonical Allele Identifier: PA2827980521
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2469Thr
CA16037620
NM_001354899.2:c.7405T>A