Canonical Allele Identifier: PA2828011637
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Lys2266Glu
CA16036732
NM_001354902.2:c.6796A>G