Canonical Allele Identifier: PA2827984746
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile984Val
CA008024
NM_001354900.2:c.2950A>G