Allele Registry

Canonical Allele Identifier: PA2825553590

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000011769

RCV003621780

ClinVar Variation:

11022

2780476

HGVS (amino-acid)	Matching Registered Transcripts
NP_001098713.1:p.Asn557Lys	CA121303 NM_001105243.2:c.1671C>G CA414002219 NM_001105243.2:c.1671C>A