Canonical Allele Identifier: PA2826156012
Gene: CLDN19 HGNC NCBI

Linked Data

ClinVar Variation Id: 297342
ClinVar RCV Id: RCV000401032
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172046.1:p.Ile113Val
CA801402
NM_001185117.2:c.337A>G