Canonical Allele Identifier: PA2825553330
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1195629
ClinVar RCV Id: RCV001558786

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Tyr275Ser
CA414007919
NM_001105243.2:c.824A>C