Canonical Allele Identifier: PA2825553465
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2074036
ClinVar RCV Id: RCV002976011 RCV003443100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Leu411Gln
CA414003541
NM_001105243.2:c.1232T>A