Canonical Allele Identifier: PA2825924964
Gene: CLDN14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2250275
ClinVar RCV Id: RCV002787201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139551.1:p.Ala135Ser
CA320313933
NM_001146079.2:c.403G>T