Canonical Allele Identifier: PA2828782777
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 5932
ClinVar RCV Id: RCV000006295
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365422.1:p.Gly163Asp
CA117865
NM_001378493.1:c.488G>A