Allele Registry

Canonical Allele Identifier: PA2826148548

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV001291527

RCV001836982

ClinVar Variation:

996747

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Asp155His	CA414009592 NM_001184880.2:c.463G>C