Allele Registry

Canonical Allele Identifier: PA316398

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000188385

RCV003621516

ClinVar Variation:

206348

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Ile101del	CA316396 NM_001184880.2:c.301_303del