Canonical Allele Identifier: PA2825553602
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 521852
ClinVar RCV Id: RCV000622974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Pro566Gln
CA414002165
NM_001105243.2:c.1697C>A