Canonical Allele Identifier: PA2828782676
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 5932
ClinVar RCV Id: RCV000006295
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365421.1:p.Gly163Asp
CA117865
NM_001378492.1:c.488G>A