Canonical Allele Identifier: PA2828782647
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 5936
ClinVar RCV Id: RCV000006299 RCV001851694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365421.1:p.Leu75Pro
CA117869
NM_001378492.1:c.224T>C