Canonical Allele Identifier: PA2499286633
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1073814
ClinVar RCV Id: RCV001386920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.Asn447Asp
CA414002949
NM_020766.3:c.1339A>G