Canonical Allele Identifier: PA109928
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 449356
ClinVar RCV Id: RCV000521156 RCV000763636
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Pro567Leu
CA414002159
NM_001184880.2:c.1700C>T