Allele Registry

Canonical Allele Identifier: PA2828782678

Gene: CLDN16 HGNC NCBI

ClinVar RCV:

RCV000006296

ClinVar Variation:

5933

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365421.1:p.Ser165Phe	CA117866 NM_001378492.1:c.494C>T