Canonical Allele Identifier: PA2825553338
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1423111
ClinVar RCV Id: RCV001926489 RCV002300623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Arg284His
CA333826084
NM_001105243.2:c.851G>A