Allele Registry

Canonical Allele Identifier: PA316347

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000188367

ClinVar Variation:

206330

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Glu414Val	CA316345 NM_001184880.2:c.1241A>T