Canonical Allele Identifier: PA316386
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 206344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Phe896Ser
CA316384
NM_001184880.2:c.2687T>C