Canonical Allele Identifier: PA2826148837
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 806017
ClinVar RCV Id: RCV001199427 RCV001322494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Tyr490Cys
CA414002661
NM_001184880.2:c.1469A>G