Canonical Allele Identifier: PA109724
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 11022
ClinVar RCV Id: RCV000011769
ClinVar Variation Id: 2780476
ClinVar RCV Id: RCV003621780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Asn557Lys
CA121303
NM_001184880.2:c.1671C>G
CA414002219
NM_001184880.2:c.1671C>A