Canonical Allele Identifier: PA1139730652
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 947804
ClinVar RCV Id: RCV001218941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.Gly296Val
CA414005077
NM_020766.3:c.887G>T