Canonical Allele Identifier: PA2827961831
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Leu2394Ile
CA047103
NM_001354897.2:c.7180T>A