Canonical Allele Identifier: PA916050148
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 420879
ClinVar RCV Id: RCV000485418
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.Tyr458His
CA16621148
NM_020766.3:c.1372T>C