Canonical Allele Identifier: PA2827983429
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Val568Ile
CA006055
NM_001354900.2:c.1702G>A