Canonical Allele Identifier: PA2826148661
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1254832
ClinVar RCV Id: RCV001659014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Gly271_Tyr275del
CA2499226256
NM_001184880.2:c.811_825del