Canonical Allele Identifier: PA2826148817
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2852648
ClinVar RCV Id: RCV003623269

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Tyr471Cys
CA414002776
NM_001184880.2:c.1412A>G