Canonical Allele Identifier: PA2825924922
Gene: CLDN14 HGNC NCBI

Linked Data

ClinVar Variation Id: 339892
ClinVar RCV Id: RCV000343853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139551.1:p.Arg32Ser
CA10650456
NM_001146079.2:c.96G>C
CA409884625
NM_001146079.2:c.96G>T