Canonical Allele Identifier: PA2825021342
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp1698Gly
CA16032465
NM_000038.6:c.5093A>G