Canonical Allele Identifier: PA2825592322
Gene: CLDN19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1361
ClinVar RCV Id: RCV000001426 RCV000823362 RCV003924792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116867.1:p.Gly20Asp
CA114955
NM_001123395.2:c.59G>A