Canonical Allele Identifier: PA2828782763
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 560390
ClinVar RCV Id: RCV000678491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365422.1:p.Gly131Glu
CA355766931
NM_001378493.1:c.392G>A