Canonical Allele Identifier: PA2826148670
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2076457
ClinVar RCV Id: RCV002972326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Thr285Met
CA414005199
NM_001184880.2:c.854C>T