Canonical Allele Identifier: PA2827959487
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala1681Thr
CA16032296
NM_001354897.2:c.5041G>A