Canonical Allele Identifier: PA2825553318
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 663581
ClinVar RCV Id: RCV000821479 RCV001199420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Glu267Lys
CA414008058
NM_001105243.2:c.799G>A