Allele Registry

Canonical Allele Identifier: PA2828001544

Gene: APC HGNC NCBI

ClinVar Variation Id: 411388

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341831.1:p.Ala1016Ser	CA16028614 NM_001354902.2:c.3046G>T