Canonical Allele Identifier: PA658808584
Gene: CLDN14 HGNC NCBI

Linked Data

ClinVar Variation Id: 504557
ClinVar RCV Id: RCV000600618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139549.1:p.Ala113Thr
CA10019283
NM_001146077.2:c.337G>A