Canonical Allele Identifier: PA2826148829
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 804055
ClinVar RCV Id: RCV000990905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Asp481Gly
CA414002718
NM_001184880.2:c.1442A>G