Allele Registry

Canonical Allele Identifier: PA916049919

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000188348

ClinVar Variation:

206312

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Ala142Pro	CA316293 NM_020766.3:c.424G>C