Canonical Allele Identifier: PA916050108
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 533852

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.Asp427Glu
CA414003264
NM_020766.3:c.1281C>G
CA414003266
NM_020766.3:c.1281C>A