Allele Registry

Canonical Allele Identifier: PA2825553281

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000768278

ClinVar Variation:

626145

HGVS (amino-acid)	Matching Registered Transcripts
NP_001098713.1:p.Pro236Leu	CA414008536 NM_001105243.2:c.707C>T