Canonical Allele Identifier: PA2827980735
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1410428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Val2533Gly
CA16038016
NM_001354899.2:c.7598T>G