Canonical Allele Identifier: PA172949
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 159556
ClinVar RCV Id: RCV000147075 RCV000735393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Arg787Cys
CA172947
NM_001184880.2:c.2359C>T