Canonical Allele Identifier: PA2825924852
Gene: CLDN14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2007924
ClinVar RCV Id: RCV002833476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139550.1:p.Thr115Ala
CA409881751
NM_001146078.3:c.343A>G