Canonical Allele Identifier: PA216232
Gene: CLDN19 HGNC NCBI

Linked Data

ClinVar Variation Id: 64478
ClinVar RCV Id: RCV000054665 RCV002496730 RCV003162429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_683763.2:p.Val224Glu
CA216231
NM_148960.3:c.671T>A