Allele Registry

Canonical Allele Identifier: PA2499286605

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV001291527

RCV001836982

ClinVar Variation:

996747

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Asp155His	CA414009592 NM_020766.3:c.463G>C