Canonical Allele Identifier: PA2828782760
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 5927
ClinVar RCV Id: RCV000006290
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365422.1:p.Gly121Arg
CA117860
NM_001378493.1:c.361G>A
CA355766251
NM_001378493.1:c.361G>C