Allele Registry

Canonical Allele Identifier: PA100399

Gene: CLDN19 HGNC NCBI

ClinVar RCV:

RCV000001427

ClinVar Variation:

1362

HGVS (amino-acid)	Matching Registered Transcripts
NP_683763.2:p.Gln57Glu	CA114956 NM_148960.3:c.169C>G