Allele Registry

Canonical Allele Identifier: PA2828782645

Gene: CLDN16 HGNC NCBI

ClinVar RCV:

RCV000656736

ClinVar Variation:

545702

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365421.1:p.Ala69Val	CA2753786 NM_001378492.1:c.206C>T