Allele Registry

Canonical Allele Identifier: PA3057485977

Gene: CLDN16 HGNC NCBI

ClinVar RCV:

RCV005035299

ClinVar Variation:

3589105

HGVS (amino-acid)	Matching Registered Transcripts
NP_006571.2:p.Pro130Arg	CA355766926 NM_006580.4:c.389C>G