Allele Registry

Canonical Allele Identifier: PA221633

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000079608

RCV001064429

ClinVar Variation:

93676

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Asn125Ser	CA221632 NM_001184880.2:c.374A>G