Allele Registry

Canonical Allele Identifier: PA2825592370

Gene: CLDN19 HGNC NCBI

ClinVar RCV:

RCV000001428

ClinVar Variation:

1363

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116867.1:p.Leu90Pro	CA114957 NM_001123395.2:c.269T>C