Canonical Allele Identifier: PA2828050792
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gly63Val
CA036174
NM_001354905.2:c.188G>T