Allele Registry

Canonical Allele Identifier: PA913201710

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000768278

ClinVar Variation:

626145

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Pro236Leu	CA414008536 NM_001184880.2:c.707C>T