Canonical Allele Identifier: PA916050054
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 447922
ClinVar RCV Id: RCV000516694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.Thr299Ile
CA333826080
NM_020766.3:c.896C>T