Canonical Allele Identifier: PA109694
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 206321
ClinVar RCV Id: RCV000188357 RCV000641136 RCV002317136
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Asn232Ser
CA316319
NM_001184880.2:c.695A>G