Canonical Allele Identifier: PA2828003931
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Leu2293Ile
CA047103
NM_001354902.2:c.6877T>A