Canonical Allele Identifier: PA2828041290
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231392

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Lys1460Met
CA039747
NM_001354904.2:c.4379A>T