Canonical Allele Identifier: PA1139730645
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 806009
ClinVar RCV Id: RCV001199415 RCV001368904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.Tyr275Cys
CA414007917
NM_020766.3:c.824A>G