Canonical Allele Identifier: PA2828019621
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gly1008Cys
CA008272
NM_001354903.2:c.3022G>T