Canonical Allele Identifier: PA2827954086
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Val2677Leu
CA16038652
NM_001354896.2:c.8029G>C
CA16038653
NM_001354896.2:c.8029G>T