Canonical Allele Identifier: PA2826148842
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1346184
ClinVar RCV Id: RCV002050048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Gln496His
CA414002620
NM_001184880.2:c.1488G>T
CA414002621
NM_001184880.2:c.1488G>C