Canonical Allele Identifier: PA188050
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184169

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gly1684Glu
CA009865
NM_001127511.3:c.5051G>A