Canonical Allele Identifier: PA2573088781
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 5933
ClinVar RCV Id: RCV000006296

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006571.2:p.Ser165Phe
CA117866
NM_006580.4:c.494C>T