Canonical Allele Identifier: PA916040481
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Glu1691Lys
CA009832
NM_001354896.2:c.5071G>A