Canonical Allele Identifier: PA2827999100
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Val2571Ile
CA014160
NM_001354901.2:c.7711G>A