Canonical Allele Identifier: PA2580160981
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_001171809.1:p.Glu910Asp
CA414000142
NM_001184880.2:c.2730G>T
CA414000143
NM_001184880.2:c.2730G>C