Allele Registry

Canonical Allele Identifier: PA105924

Gene: CLDN14 HGNC NCBI

ClinVar RCV:

RCV000169749

ClinVar Variation:

189333

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139549.1:p.Gly232Arg	CA199226 NM_001146077.2:c.694G>A CA409880313 NM_001146077.2:c.694G>C