Allele Registry

Canonical Allele Identifier: PA2825553597

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV001323634

ClinVar Variation:

1023566

HGVS (amino-acid)	Matching Registered Transcripts
NP_001098713.1:p.Pro561Leu	CA414002193 NM_001105243.2:c.1682C>T