Canonical Allele Identifier: PA2829670806
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 5931
ClinVar RCV Id: RCV000006294 RCV000662319
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006571.2:p.Phe162Cys
CA117864
NM_006580.4:c.485T>G