Canonical Allele Identifier: PA2573088780
Gene: CLDN16 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006571.2:p.Gly163Asp
CA117865
NM_006580.4:c.488G>A