Canonical Allele Identifier: PA2828782661
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 802037
ClinVar RCV Id: RCV000987375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365421.1:p.Gly128Arg
CA355766290
NM_001378492.1:c.382G>C