Canonical Allele Identifier: PA2826148841
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1515439
ClinVar RCV Id: RCV002021094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Ser495Pro
CA414002632
NM_001184880.2:c.1483T>C