Allele Registry

Canonical Allele Identifier: PA2828782762

Gene: CLDN16 HGNC NCBI

ClinVar Allele:

20967

ClinVar RCV:

RCV000006291

ClinVar Variation:

5928

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365422.1:p.Gly128Asp	CA117861 NM_001378493.1:c.383G>A