Allele Registry

Canonical Allele Identifier: PA2825592351

Gene: CLDN19 HGNC NCBI

ClinVar RCV:

RCV000001427

ClinVar Variation:

1362

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116867.1:p.Gln57Glu	CA114956 NM_001123395.2:c.169C>G