Canonical Allele Identifier: PA2825021641
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Lys1770Glu
CA041323
NM_000038.6:c.5308A>G