Canonical Allele Identifier: PA658678341
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 451251
ClinVar RCV Id: RCV000523094 RCV001199428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Tyr490Ser
CA414002662
NM_001184880.2:c.1469A>C