Canonical Allele Identifier: PA2573088765
Gene: CLDN16 HGNC NCBI
ClinVar Allele:
20968
ClinVar RCV:
RCV000006292
ClinVar Variation:
5929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006571.2:p.Met1Arg