Canonical Allele Identifier: PA658682077
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly267Glu
CA049608
NM_001127510.3:c.800G>A