Canonical Allele Identifier: PA2825553810
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2129183
ClinVar RCV Id: RCV003057950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Glu863Asp
CA414000142
NM_001105243.2:c.2589G>T
CA414000143
NM_001105243.2:c.2589G>C