Canonical Allele Identifier: PA2827969539
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1171348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr1922Ile
CA16034105
NM_001354898.2:c.5765C>T