Canonical Allele Identifier: PA2828049060
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1692406

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Glu2536Gln
CA16038670
NM_001354904.2:c.7606G>C