Canonical Allele Identifier: PA2827995537
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Lys1484Glu
CA10578378
NM_001354901.2:c.4450A>G