Canonical Allele Identifier: PA1139730939
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 863992
ClinVar RCV Id: RCV001071081
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.Tyr505Cys
CA414002562
NM_020766.3:c.1514A>G