Canonical Allele Identifier: PA2827971785
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Val2605Ile
CA014160
NM_001354898.2:c.7813G>A