Canonical Allele Identifier: PA2826148536
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 860204
ClinVar RCV Id: RCV001066474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Glu140Gly
CA414009780
NM_001184880.2:c.419A>G