Allele Registry

Canonical Allele Identifier: PA645486018

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000476281

RCV000480604

ClinVar Variation:

408904

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Pro236Arg	CA16616407 NM_001184880.2:c.707C>G