Canonical Allele Identifier: PA645399339
Gene: CLDN14 HGNC NCBI

Linked Data

ClinVar Variation Id: 228520
ClinVar RCV Id: RCV000215729 RCV002291596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139549.1:p.Asp187Tyr
CA10019232
NM_001146077.2:c.559G>T