Allele Registry

Canonical Allele Identifier: PA172967

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000147084

ClinVar Variation:

159561

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Asn232Ile	CA172965 NM_001184880.2:c.695A>T