Canonical Allele Identifier: PA2825553201
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1304240
ClinVar RCV Id: RCV001752007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Asn171Lys
CA414009464
NM_001105243.2:c.513C>A
CA414009465
NM_001105243.2:c.513C>G