Allele Registry

Canonical Allele Identifier: PA109909

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV002009343

ClinVar Variation:

1507139

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Pro344Arg	CA414004645 NM_001184880.2:c.1031C>G