Canonical Allele Identifier: PA2828782654
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 5930
ClinVar RCV Id: RCV000006293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365421.1:p.Leu97Pro
CA117863
NM_001378492.1:c.290T>C