Canonical Allele Identifier: PA2828027900
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1022071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Lys2129Glu
CA16037088
NM_001354906.2:c.6385A>G