Canonical Allele Identifier: PA2827999025
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760781
ClinVar RCV Id: RCV002410000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Lys2550Glu
CA16038330
NM_001354901.2:c.7648A>G