Allele Registry

Canonical Allele Identifier: PA2826148780

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV001350410

ClinVar Variation:

1045922

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Glu414Lys	CA414003512 NM_001184880.2:c.1240G>A