Canonical Allele Identifier: PA2825553513
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2852648
ClinVar RCV Id: RCV003623269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Tyr471Cys
CA414002776
NM_001105243.2:c.1412A>G