Canonical Allele Identifier: PA2825553198
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2765982
ClinVar RCV Id: RCV003510279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Tyr166Asp
CA414009500
NM_001105243.2:c.496T>G