Canonical Allele Identifier: PA2825018905
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp1133Glu
CA16028782
NM_000038.6:c.3399T>A
CA16028783
NM_000038.6:c.3399T>G