Canonical Allele Identifier: PA2826155972
Gene: CLDN19 HGNC NCBI

Linked Data

ClinVar Variation Id: 297346
ClinVar RCV Id: RCV000302592 RCV001052078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172046.1:p.Ile22Thr
CA801482
NM_001185117.2:c.65T>C