Canonical Allele Identifier: PA2825019793
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val1320Glu
CA037191
NM_000038.6:c.3959T>A