Canonical Allele Identifier: PA2825553299
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2978427
ClinVar RCV Id: RCV003837089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Asn254Lys
CA414008263
NM_001105243.2:c.762C>G
CA414008265
NM_001105243.2:c.762C>A