Canonical Allele Identifier: PA2827978137
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys1740Glu
CA010041
NM_001354899.2:c.5218A>G