Allele Registry

Canonical Allele Identifier: PA105939

Gene: CLDN14 HGNC NCBI

ClinVar RCV:

RCV000005124

RCV000417186

RCV001291511

ClinVar Variation:

4851

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139549.1:p.Val85Asp	CA117103 NM_001146077.2:c.254T>A