Allele Registry

Canonical Allele Identifier: PA2828782679

Gene: CLDN16 HGNC NCBI

ClinVar RCV:

RCV001780794

ClinVar Variation:

1324089

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365421.1:p.Ser165Tyr	CA355767154 NM_001378492.1:c.494C>A