Allele Registry

Canonical Allele Identifier: PA2826148653

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000821479

RCV001199420

ClinVar Variation:

663581

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Glu267Lys	CA414008058 NM_001184880.2:c.799G>A