Canonical Allele Identifier: PA2827980742
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2566987
ClinVar RCV Id: RCV003278281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Trp2536Gly
CA16038033
NM_001354899.2:c.7606T>G