Canonical Allele Identifier: PA2827974063
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr490Met
CA028394
NM_001354899.2:c.1469C>T