Canonical Allele Identifier: PA2828008930
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gln1792Glu
CA16034137
NM_001354905.2:c.5374C>G