Canonical Allele Identifier: PA2829954171
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 206344
ClinVar RCV Id: RCV000188381 RCV000801633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.Phe848Ser
CA316384
NM_020766.3:c.2543T>C