Canonical Allele Identifier: PA658832871
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 546369
ClinVar RCV Id: RCV000658233 RCV001861692
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Val300Ala
CA414005058
NM_001184880.2:c.899T>C