Canonical Allele Identifier: PA2825553494
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1432398
ClinVar RCV Id: RCV001959857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.His450Pro
CA414002918
NM_001105243.2:c.1349A>C