Canonical Allele Identifier: PA2825553564
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2793170
ClinVar RCV Id: RCV003621929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.His523Gln
CA414002440
NM_001105243.2:c.1569C>G
CA414002441
NM_001105243.2:c.1569C>A