Canonical Allele Identifier: PA2828040955
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Lys1417Glu
CA10578378
NM_001354904.2:c.4249A>G