Canonical Allele Identifier: PA2828006734
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231392

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Lys1426Met
CA039747
NM_001354905.2:c.4277A>T