Canonical Allele Identifier: PA221631
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 93674
ClinVar RCV Id: RCV000188321 RCV000641140 RCV002316235 RCV001537807 RCV003952500
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Pro1079Ala
CA221629
NM_001184880.2:c.3235C>G