Canonical Allele Identifier: PA2827998877
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Val2502Ile
CA16038011
NM_001354901.2:c.7504G>A