Canonical Allele Identifier: PA2825553556
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1450724
ClinVar RCV Id: RCV002014840

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Gly513Asp
CA414002509
NM_001105243.2:c.1538G>A