Canonical Allele Identifier: PA2828020811
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Val1037Glu
CA037191
NM_001354906.2:c.3110T>A