Canonical Allele Identifier: PA2828029547
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Val2376Leu
CA16038652
NM_001354906.2:c.7126G>C
CA16038653
NM_001354906.2:c.7126G>T