Canonical Allele Identifier: PA2825025106
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411376

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp2663Gly
CA16038681
NM_000038.6:c.7988A>G