Canonical Allele Identifier: PA109920
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 206337

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Pro561Arg
CA316366
NM_001184880.2:c.1682C>G