Canonical Allele Identifier: PA2828006582
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Lys1383Glu
CA10578378
NM_001354905.2:c.4147A>G