Canonical Allele Identifier: PA2828043793
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482259

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Lys1767Glu
CA042579
NM_001354904.2:c.5299A>G