Canonical Allele Identifier: PA2827989134
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Lys2316Glu
CA16036732
NM_001354900.2:c.6946A>G