Canonical Allele Identifier: PA2827980057
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys2329Glu
CA16036732
NM_001354899.2:c.6985A>G