Canonical Allele Identifier: PA2826148660
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1015597
ClinVar RCV Id: RCV001314479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Gly271Ser
CA414007989
NM_001184880.2:c.811G>A