Canonical Allele Identifier: PA2827947737
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Val2561Ile
CA16038011
NM_001354895.2:c.7681G>A