Canonical Allele Identifier: PA2825553349
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1308418
ClinVar RCV Id: RCV001763330

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Gly296Ser
CA10468939
NM_001105243.2:c.886G>A