Canonical Allele Identifier: PA2828782662
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 5928
ClinVar RCV Id: RCV000006291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365421.1:p.Gly128Asp
CA117861
NM_001378492.1:c.383G>A