Canonical Allele Identifier: PA2826148866
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2102799
ClinVar RCV Id: RCV003019696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Leu534Pro
CA414002362
NM_001184880.2:c.1601T>C