Allele Registry

Canonical Allele Identifier: PA2573088770

Gene: CLDN16 HGNC NCBI

ClinVar RCV:

RCV000656736

ClinVar Variation:

545702

HGVS (amino-acid)	Matching Registered Transcripts
NP_006571.2:p.Ala69Val	CA2753786 NM_006580.4:c.206C>T