Allele Registry

Canonical Allele Identifier: PA2828782654

Gene: CLDN16 HGNC NCBI

ClinVar Allele:

20969

ClinVar RCV:

RCV000006293

ClinVar Variation:

5930

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365421.1:p.Leu97Pro	CA117863 NM_001378492.1:c.290T>C