Canonical Allele Identifier: PA2829954087
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_065817.2:p.Arg740Cys
CA172947
NM_020766.3:c.2218C>T