Canonical Allele Identifier: PA2826156002
Gene: CLDN19 HGNC NCBI
ClinVar RCV:
RCV000001428
ClinVar Variation:
1363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172046.1:p.Leu90Pro
CA114957
NM_001185117.2:c.269T>C