Canonical Allele Identifier: PA2827989316
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1022071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Lys2371Glu
CA16037088
NM_001354900.2:c.7111A>G