Allele Registry

Canonical Allele Identifier: PA2828782707

Gene: CLDN16 HGNC NCBI

ClinVar RCV:

RCV002665652

ClinVar Variation:

2216171

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365421.1:p.Thr233Lys	CA355768841 NM_001378492.1:c.698C>A