Canonical Allele Identifier: PA2827989812
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Val2520Ile
CA16038011
NM_001354900.2:c.7558G>A