Canonical Allele Identifier: PA2499286618
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1254832
ClinVar RCV Id: RCV001659014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.Gly271_Tyr275del
CA2499226256
NM_020766.3:c.811_825del