Canonical Allele Identifier: PA316349
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 206331
ClinVar RCV Id: RCV000188368 RCV001199422
ClinVar Variation Id: 408903
ClinVar RCV Id: RCV000470577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Asp445Glu
CA316348
NM_001105243.2:c.1335C>A
CA16616395
NM_001105243.2:c.1335C>G