Canonical Allele Identifier: PA221630
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 93674
ClinVar RCV Id: RCV000188321 RCV000641140 RCV002316235 RCV001537807 RCV003952500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Pro1032Ala
CA221629
NM_001105243.2:c.3094C>G