Canonical Allele Identifier: PA2828013343
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Val2499Leu
CA16038652
NM_001354905.2:c.7495G>C
CA16038653
NM_001354905.2:c.7495G>T