Canonical Allele Identifier: PA2825553332
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 579744
ClinVar RCV Id: RCV000703107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Ser276del
CA891843595
NM_001105243.2:c.827_829del