Canonical Allele Identifier: PA916050152
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 432615
ClinVar RCV Id: RCV001697003 RCV001857019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.Val462Met
CA10468891
NM_020766.3:c.1384G>A