Allele Registry

Canonical Allele Identifier: PA2826155990

Gene: CLDN19 HGNC NCBI

ClinVar RCV:

RCV000001427

ClinVar Variation:

1362

HGVS (amino-acid)	Matching Registered Transcripts
NP_001172046.1:p.Gln57Glu	CA114956 NM_001185117.2:c.169C>G