Allele Registry

Canonical Allele Identifier: PA117105

Gene: CLDN14 HGNC NCBI

ClinVar RCV:

RCV000005125

RCV001762034

ClinVar Variation:

4852

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139549.1:p.Gly101Arg	CA117104 NM_001146077.2:c.301G>A CA409882044 NM_001146077.2:c.301G>C