Allele Registry

Canonical Allele Identifier: PA2828782708

Gene: CLDN16 HGNC NCBI

ClinVar RCV:

RCV000006302

ClinVar Variation:

5939

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365421.1:p.Thr233Arg	CA117872 NM_001378492.1:c.698C>G