Canonical Allele Identifier: PA2828782753
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 5935
ClinVar RCV Id: RCV000006298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365422.1:p.Leu81Trp
CA117868
NM_001378493.1:c.242T>G