Canonical Allele Identifier: PA2573280675
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1432398
ClinVar RCV Id: RCV001959857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.His450Pro
CA414002918
NM_020766.3:c.1349A>C