Canonical Allele Identifier: PA2828046956
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Gly2244Val
CA046963
NM_001354904.2:c.6731G>T