Allele Registry

Canonical Allele Identifier: PA916050043

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000821479

RCV001199420

ClinVar Variation:

663581

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Glu267Lys	CA414008058 NM_020766.3:c.799G>A