Canonical Allele Identifier: PA2828026702
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Glu2107Ala
CA045546
NM_001354903.2:c.6320A>C