Canonical Allele Identifier: PA2826148820
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2158657
ClinVar RCV Id: RCV003069876
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Ser476Phe
CA414002746
NM_001184880.2:c.1427C>T