Canonical Allele Identifier: PA2825013833
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly267Glu
CA049608
NM_000038.6:c.800G>A