Canonical Allele Identifier: PA658678311
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 447922
ClinVar RCV Id: RCV000516694
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Thr299Ile
CA333826080
NM_001184880.2:c.896C>T