Allele Registry

Canonical Allele Identifier: PA2828782660

Gene: CLDN16 HGNC NCBI

ClinVar RCV:

RCV000006290

ClinVar Variation:

5927

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365421.1:p.Gly121Arg	CA117860 NM_001378492.1:c.361G>A CA355766251 NM_001378492.1:c.361G>C