Allele Registry

Canonical Allele Identifier: PA316285

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000188345

ClinVar Variation:

206309

HGVS (amino-acid)	Matching Registered Transcripts
NP_001098713.1:p.Asp121His	CA316284 NM_001105243.2:c.361G>C