Canonical Allele Identifier: PA2825592416
Gene: CLDN19 HGNC NCBI

Linked Data

ClinVar Variation Id: 297340
ClinVar RCV Id: RCV000295255 RCV001516776
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116867.1:p.Arg200Gln
CA801335
NM_001123395.2:c.599G>A