Allele Registry

Canonical Allele Identifier: PA133523

Gene: CLDN14 HGNC NCBI

ClinVar RCV:

RCV000037059

RCV000991809

RCV001000269

ClinVar Variation:

44083

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139549.1:p.Thr4Met	CA133522 NM_001146077.2:c.11C>T