Canonical Allele Identifier: PA2827996302
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Val1717Ile
CA041569
NM_001354901.2:c.5149G>A