Canonical Allele Identifier: PA2826148830
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1364705
ClinVar RCV Id: RCV001942477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Asp481Glu
CA414002715
NM_001184880.2:c.1443C>A
CA414002716
NM_001184880.2:c.1443C>G