Canonical Allele Identifier: PA2825924733
Gene: CLDN14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1064914
ClinVar RCV Id: RCV001375125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139549.1:p.His57Tyr
CA10019330
NM_001146077.2:c.169C>T