Canonical Allele Identifier: PA2826148686
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019037
ClinVar RCV Id: RCV001318419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Glu308Lys
CA10468937
NM_001184880.2:c.922G>A