Allele Registry

Canonical Allele Identifier: PA316289

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000188346

RCV000494296

RCV002524035

RCV003621514

ClinVar Variation:

206310

429767

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Asn123Lys	CA316287 NM_001184880.2:c.369C>A CA414010286 NM_001184880.2:c.369C>G