Canonical Allele Identifier: PA166133
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Glu1191Lys
CA008564
NM_001127511.3:c.3571G>A