Canonical Allele Identifier: PA2825025699
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr2813Lys
CA16039637
NM_000038.6:c.8438C>A