Canonical Allele Identifier: PA2828046891
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Lys2231Glu
CA16036732
NM_001354904.2:c.6691A>G