Canonical Allele Identifier: PA2573253151
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 1464906
ClinVar RCV Id: RCV001979241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006571.2:p.Ala139Thr
CA355766978
NM_006580.4:c.415G>A