Canonical Allele Identifier: PA2499286620
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1195629
ClinVar RCV Id: RCV001558786

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.Tyr275Ser
CA414007919
NM_020766.3:c.824A>C