Canonical Allele Identifier: PA2825553516
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2158657
ClinVar RCV Id: RCV003069876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Ser476Phe
CA414002746
NM_001105243.2:c.1427C>T