Canonical Allele Identifier: PA658688882
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Lys2357Glu
CA16036732
NM_001127510.3:c.7069A>G