ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826148523
Gene: PCDH19
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV001213098
RCV001819902
RCV003235500
ClinVar Variation:
943000
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001171809.1:p.Asp124His
CA414010276
NM_001184880.2:c.370G>C