Canonical Allele Identifier: PA2825924868
Gene: CLDN14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1810054
ClinVar RCV Id: RCV002508610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139550.1:p.Ser154Arg
CA409881487
NM_001146078.3:c.462C>G
CA409881488
NM_001146078.3:c.462C>A
CA409881493
NM_001146078.3:c.460A>C