Canonical Allele Identifier: PA2828782660
Gene: CLDN16 HGNC NCBI

Linked Data

ClinVar Variation Id: 5927
ClinVar RCV Id: RCV000006290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365421.1:p.Gly121Arg
CA117860
NM_001378492.1:c.361G>A
CA355766251
NM_001378492.1:c.361G>C