Canonical Allele Identifier: PA216269
Gene: CLDN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64495
ClinVar RCV Id: RCV000054682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164563.1:p.Asp65His
CA216268
NM_001171092.1:c.193G>C